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Table 4 The information of the 9 fetus hypermethylation DNA markers (FH) and 12 fetus hypomethylation DNA markers (FL)

From: DNA methylation study of fetus genome through a genome-wide analysis

Marker ID Chromosomal locition Associated gene
FH1 ChrM:1-542 Mitochondrial DNA D-loop
FH2 ChrM:16,025-16,571 Mitochondrial DNA D-loop
FH3 Chr19:40,628,281-40,629,300 Free fatty acid receptor 2 (FFAR2)
FH4 Chr21:38,791,600-38,792,000 Erythroblastosis virus E26 oncogene onmcogene homolog (ERG)
FH5 Chr7:2,411,800-2,412,100 Carbohydrate (chondroitin 4) Sulfotransferase 12 (CHST12)
FH6 Chr12:6,528,400-6,528,750 Intermediate filament family orphan 1 (IFFO1)
FH7 Chr9:129,579,800-129,580,000 SH2 domain containing 3C (SH2D3C)
FH8 Chr17:36,717,500-36,717,900 Keratin associated protein 16-1 (KRTAP16-1)
FH9 Chr19:1,019,900-1,020,200 Histocompatibility (minor) HA-1 (HMHA1)
FL1 Chr7:27,130,100-27,130,600 Homeobox A3 (HOXA3)
FL2 Chr11:62127350-62127700 Echinoderm microtubule associated protein like 3 (EML3)
FL3 Chr3:32,835,500-32,835,800 Tripartite motif containing 71, E3 ubiquitin protein ligase (TRIM71)
FL4 Chr7:27,185,300-27,185,650 Homo sapiens homeobox A11 (HOXA11)
FL5 Chr6:10,664,250-10,664,600 Homo sapiens glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (GCNT2)
FL6 Chr7:27,113,100-27,113,300 Homo sapiens homeobox A2 (HOXA2)
FL7 Chr7:27,148,050-27,148,400 Homeobox A5 (HOXA5)
FL8 Chr19:12,997,300-12,997,450 Nuclear factor I/X (NFIX) (CCAAT-binding transcription factor)
FL9 Chr8:116,753,900-116,754,200 Homo sapiens trichorhinophalangeal syndrome I (TRPS1)
FL10 Chr5:95,321,600-95,321,800 Elongation factor, RNA polymerase II, 2 (ELL2)
FL11 Chr7:32,213,400-32,213,600 Phosphodiesterase 1C, calmodulin-dependent (PDE1C)
FL12 Chr8:82,066,300-82,066,500 Phosphoprotein associated with glycosphingolipid microdomains 1 (PAG1)