| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119468848-119469014 | Rare:63 | ||||
| chr3:119498406-119498954 | Common:4; Rare:188 | ||||
| chr3:119677373-119677524 | Rare:49 | ||||
| chr3:120093501-120093766 | Rare:67 | ||||
| chr3:120093773-120093966 | Common:1; Rare:67 | ||||
| chr3:120094414-120094775 | Common:4; Rare:115 | ||||
| chr3:120402732-120402921 | Common:1; Rare:44 | ||||
| chr3:120450881-120451084 | Rare:68 | ||||
| chr3:120451134-120451356 | Rare:57 | ||||
| chr3:120595994-120596473 | Common:3; Rare:166 | ||||
| chr3:120742483-120742832 | Common:2; Rare:99 | ||||
| chr3:121749209-121749266 | Rare:12 | ||||
| chr3:121749627-121749795 | Rare:37 | ||||
| chr3:121749909-121749994 | Common:1; Rare:19 | ||||
| chr3:121834975-121835257 | Common:3; Rare:96; Clinvar:6; Clinvar (benign):2 |