| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143823953-143824167 | Common:1; Rare:56 | ||||
| chr8:143829295-143829579 | Rare:118 | ||||
| chr8:143840924-143841268 | Rare:86 | ||||
| chr8:143953807-143954030 | Common:3; Rare:64 | ||||
| chr8:143989933-143990141 | Common:1; Rare:79 | ||||
| chr8:143990908-143991852 | Common:1; Rare:448 | ||||
| chr8:144078534-144078746 | Common:1; Rare:65 | ||||
| chr8:144079047-144079180 | Rare:32 | ||||
| chr8:144082360-144082700 | Common:2; Rare:99 | ||||
| chr8:144094938-144095133 | Common:2; Rare:65; Clinvar (benign):1 | ||||
| chr8:144103680-144103872 | Common:1; Rare:69 | ||||
| chr8:144104159-144104550 | Common:3; Rare:137 | ||||
| chr8:144137598-144137832 | Common:2; Rare:66 | ||||
| chr8:144138090-144138490 | Rare:85 | ||||
| chr8:144147727-144148036 | Common:2; Rare:82 |