Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:119366742-119367048 | Common:1; Rare:90 | ||||
chr2:119759785-119760022 | Common:2; Rare:72 | ||||
chr2:120252614-120252964 | Common:3; Rare:115 | ||||
chr2:121530574-121530939 | Common:7; Rare:201; Clinvar (pathogenic):11 | ||||
chr2:121649521-121649816 | Rare:78 | ||||
chr2:121649932-121650188 | Common:1; Rare:70 | ||||
chr2:121736867-121737105 | Common:4; Rare:76 | ||||
chr2:126656032-126656312 | Common:1; Rare:84; Clinvar:2 | ||||
chr2:127294137-127294219 | Common:2; Rare:25; Clinvar (benign):2 | ||||
chr2:127811150-127811301 | Common:1; Rare:54 | ||||
chr2:127858089-127858205 | Common:1; Rare:65 | ||||
chr2:127885928-127885975 | Rare:7 | ||||
chr2:130181549-130181704 | Common:1; Rare:54 | ||||
chr2:130182089-130182279 | Common:1; Rare:68 | ||||
chr2:130342129-130342242 | Rare:44 |