| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:134713025-134713205 | Common:1; Rare:65 | ||||
| chr8:140511252-140511494 | Common:2; Rare:99 | ||||
| chr8:141001136-141001496 | Common:4; Rare:126 | ||||
| chr8:143018432-143018565 | Common:1; Rare:37 | ||||
| chr8:143829306-143829566 | Rare:115 | ||||
| chr8:143939511-143939780 | Common:3; Rare:77 | ||||
| chr8:144078532-144078715 | Common:1; Rare:56 | ||||
| chr8:144413542-144413718 | Rare:56; Clinvar:1 | ||||
| chr9:4679437-4679710 | Common:1; Rare:119 | ||||
| chr9:6015606-6015732 | Rare:56 | ||||
| chr9:15422596-15422888 | Common:1; Rare:128 | ||||
| chr9:19380184-19380354 | Common:4; Rare:82 | ||||
| chr9:20684032-20684282 | Common:4; Rare:96 | ||||
| chr9:21802323-21802687 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21994301-21994736 | Common:2; Rare:125; Clinvar:4; Clinvar (benign):6 |