| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:43056200-43056476 | Rare:107 | ||||
| chr8:43140284-43140572 | Common:3; Rare:114; Clinvar:9 | ||||
| chr8:47260781-47260989 | Common:3; Rare:92 | ||||
| chr8:47960064-47960263 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):3 | ||||
| chr8:47960683-47961004 | Common:2; Rare:122; Clinvar:10; Clinvar (benign):1 | ||||
| chr8:48008319-48008467 | Common:2; Rare:91 | ||||
| chr8:51898984-51899347 | Common:7; Rare:162 | ||||
| chr8:51899554-51899675 | Rare:26 | ||||
| chr8:52714377-52714611 | Common:1; Rare:105 | ||||
| chr8:53843207-53843358 | Rare:37 | ||||
| chr8:53880810-53880888 | Rare:22 | ||||
| chr8:54021916-54022061 | Rare:67 | ||||
| chr8:54022067-54022162 | Rare:36 | ||||
| chr8:54022246-54022545 | Common:1; Rare:99 | ||||
| chr8:54101765-54102156 | Common:3; Rare:159 |