| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:125091631-125091923 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:127735895-127736086 | Rare:44 | ||||
| chr8:130016608-130016790 | Common:2; Rare:56 | ||||
| chr8:133060294-133060502 | Rare:48 | ||||
| chr8:134713025-134713260 | Common:1; Rare:84 | ||||
| chr8:140511252-140511526 | Common:2; Rare:110 | ||||
| chr8:141001136-141001478 | Common:3; Rare:119 | ||||
| chr8:142669941-142670270 | Common:8; Rare:122 | ||||
| chr8:143334831-143334966 | Common:1; Rare:47 | ||||
| chr8:143541417-143541636 | Common:2; Rare:74 | ||||
| chr8:143558267-143558394 | Common:1; Rare:52 | ||||
| chr8:143617464-143617759 | Common:2; Rare:111 | ||||
| chr8:143635893-143636040 | Common:1; Rare:61 | ||||
| chr8:143684364-143684494 | Common:2; Rare:26 | ||||
| chr8:143829310-143829500 | Rare:72 |