| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:97868911-97869148 | Common:1; Rare:48 | ||||
| chr8:98042698-98042885 | Common:1; Rare:33 | ||||
| chr8:98045333-98045676 | Common:4; Rare:101 | ||||
| chr8:98117144-98117325 | Common:2; Rare:61 | ||||
| chr8:99013008-99013339 | Rare:66 | ||||
| chr8:100150564-100150709 | Rare:44 | ||||
| chr8:100233251-100233467 | Common:1; Rare:49; Clinvar (pathogenic):1 | ||||
| chr8:100309826-100310184 | Rare:107 | ||||
| chr8:100336155-100336353 | Common:1; Rare:38 | ||||
| chr8:100706649-100707012 | Common:10; Rare:95 | ||||
| chr8:100709108-100709733 | Common:11; Rare:156 | ||||
| chr8:100950411-100950706 | Common:11; Rare:123 | ||||
| chr8:100950709-100950756 | Common:1; Rare:11 | ||||
| chr8:100951270-100951420 | Rare:53 | ||||
| chr8:100951595-100951809 | Common:1; Rare:74 |