| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119872821-119873090 | Common:4; Rare:97 | ||||
| chr10:119892488-119892777 | Common:3; Rare:104 | ||||
| chr10:120851200-120851515 | Common:6; Rare:113 | ||||
| chr10:121927957-121928195 | Common:1; Rare:62 | ||||
| chr10:121928429-121928522 | Rare:27 | ||||
| chr10:121974792-121974898 | Rare:40 | ||||
| chr10:121975172-121975406 | Common:1; Rare:44 | ||||
| chr10:122019717-122019821 | Common:2; Rare:10 | ||||
| chr10:122112457-122112754 | Common:2; Rare:57 | ||||
| chr10:122290827-122291144 | Common:4; Rare:67 | ||||
| chr10:122374658-122374806 | Rare:64 | ||||
| chr10:122375187-122375436 | Common:2; Rare:72 | ||||
| chr10:122461963-122462119 | Rare:41; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr10:122879488-122879758 | Common:4; Rare:70 | ||||
| chr10:122954179-122954479 | Rare:109 |