Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:106316169-106316607 | Common:5; Rare:140 | ||||
chr4:107989694-107989860 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):2 | ||||
chr4:108620487-108620659 | Common:4; Rare:89 | ||||
chr4:108650701-108650789 | Rare:30 | ||||
chr4:109433738-109433933 | Common:1; Rare:64 | ||||
chr4:109815163-109815807 | Common:3; Rare:166 | ||||
chr4:112145313-112145454 | Rare:31 | ||||
chr4:112231570-112231844 | Common:2; Rare:89 | ||||
chr4:112285767-112285947 | Rare:57 | ||||
chr4:112636846-112637228 | Common:2; Rare:106 | ||||
chr4:112637390-112637570 | Common:3; Rare:47 | ||||
chr4:113979678-113979707 | Rare:7 | ||||
chr4:118352969-118353246 | Rare:82 | ||||
chr4:118685318-118685501 | Common:2; Rare:53 | ||||
chr4:118835663-118835796 | Common:2; Rare:20 |