| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:98045503-98045642 | Common:2; Rare:47 | ||||
| chr8:98117164-98117315 | Common:2; Rare:47 | ||||
| chr8:99012951-99013357 | Rare:85; Clinvar:1 | ||||
| chr8:100709130-100709714 | Common:11; Rare:143 | ||||
| chr8:100712878-100713233 | Common:9; Rare:91 | ||||
| chr8:100718270-100718405 | Rare:35 | ||||
| chr8:100721748-100722102 | Common:1; Rare:114 | ||||
| chr8:100950427-100950709 | Common:10; Rare:119 | ||||
| chr8:100951708-100952199 | Common:2; Rare:171 | ||||
| chr8:102239026-102239389 | Common:5; Rare:81; Clinvar (benign):1 | ||||
| chr8:103415104-103415445 | Common:6; Rare:175 | ||||
| chr8:106657578-106657878 | Common:3; Rare:74 | ||||
| chr8:109334074-109334405 | Common:1; Rare:83 | ||||
| chr8:116766266-116766524 | Common:4; Rare:61 | ||||
| chr8:116874612-116874931 | Common:6; Rare:134; Clinvar (benign):1 |