| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:96261574-96261957 | Common:5; Rare:128 | ||||
| chr8:98045499-98045653 | Common:2; Rare:51 | ||||
| chr8:98117120-98117340 | Common:4; Rare:71 | ||||
| chr8:99013007-99013355 | Rare:74; Clinvar:1 | ||||
| chr8:100150551-100150689 | Rare:46 | ||||
| chr8:102655619-102655871 | Common:1; Rare:96 | ||||
| chr8:103298730-103298944 | Common:2; Rare:52 | ||||
| chr8:103415007-103415503 | Common:6; Rare:245 | ||||
| chr8:109334051-109334416 | Common:1; Rare:94 | ||||
| chr8:116766319-116766540 | Common:4; Rare:52 | ||||
| chr8:117520540-117520778 | Common:5; Rare:60 | ||||
| chr8:118951920-118952259 | Common:1; Rare:82; Clinvar:6; Clinvar (benign):1 | ||||
| chr8:119832794-119832897 | Common:1; Rare:46 | ||||
| chr8:119873540-119873877 | Common:3; Rare:96 | ||||
| chr8:120445087-120445420 | Common:1; Rare:78 |