| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:47959972-47959987 | Rare:4 | ||||
| chr8:47960122-47960191 | Rare:24; Clinvar (benign):1 | ||||
| chr8:47960668-47961000 | Common:2; Rare:129; Clinvar:11; Clinvar (benign):1 | ||||
| chr8:48008327-48008457 | Common:2; Rare:81 | ||||
| chr8:51898995-51899277 | Common:5; Rare:132 | ||||
| chr8:51899527-51899649 | Rare:26 | ||||
| chr8:52714174-52714603 | Common:2; Rare:162 | ||||
| chr8:53843226-53843318 | Rare:21 | ||||
| chr8:54022133-54022543 | Common:1; Rare:138 | ||||
| chr8:54101773-54102139 | Common:3; Rare:151 | ||||
| chr8:54135153-54135290 | Common:2; Rare:47 | ||||
| chr8:55773306-55773506 | Common:3; Rare:68 | ||||
| chr8:55879669-55879950 | Rare:57 | ||||
| chr8:56074384-56074602 | Common:4; Rare:106 | ||||
| chr8:58411264-58411413 | Common:2; Rare:47 |