| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:119151816-119152049 | Common:3; Rare:47 | ||||
| chr8:123534769-123534980 | Rare:34 | ||||
| chr8:123914351-123914652 | Common:2; Rare:46 | ||||
| chr8:125951148-125951408 | Common:2; Rare:42 | ||||
| chr8:133072263-133072369 | Common:1; Rare:15 | ||||
| chr8:133295007-133295346 | Common:1; Rare:73 | ||||
| chr8:141185064-141185187 | Rare:28 | ||||
| chr8:141225196-141225471 | Common:1; Rare:56 | ||||
| chr8:141276422-141276709 | Common:3; Rare:49 | ||||
| chr8:141278083-141278225 | Rare:19 | ||||
| chr8:143805347-143805592 | Common:5; Rare:71 | ||||
| chr8:143816757-143817130 | Common:2; Rare:121; Clinvar:1 | ||||
| chr8:143930003-143930306 | Common:3; Rare:127; Clinvar:16; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr8:143937258-143937533 | Rare:75 | ||||
| chr8:143938215-143938263 | Rare:18; Clinvar:1; Clinvar (benign):2 |