Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:72334654-72334942 | Common:1; Rare:45 | ||||
chr3:74368889-74369187 | Rare:62 | ||||
chr3:75305910-75306138 | Common:4; Rare:50 | ||||
chr3:75435021-75435372 | Common:4; Rare:123 | ||||
chr3:75641092-75641403 | Common:1; Rare:47 | ||||
chr3:75672097-75672267 | Common:15; Rare:6 | ||||
chr3:75672569-75672754 | Rare:1 | ||||
chr3:80770281-80770669 | Common:7; Rare:114 | ||||
chr3:80771168-80771347 | Common:2; Rare:52 | ||||
chr3:81761197-81761295 | Rare:23 | ||||
chr3:81761523-81761609 | Common:5; Rare:25; Clinvar (benign):1 | ||||
chr3:98734813-98734962 | Common:1; Rare:27 | ||||
chr3:100682967-100683077 | Rare:21 | ||||
chr3:101576975-101577093 | Common:1; Rare:33 | ||||
chr3:101676267-101676514 | Common:2; Rare:85 |