| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143684387-143684524 | Common:4; Rare:27 | ||||
| chr8:143829009-143829149 | Common:1; Rare:54 | ||||
| chr8:143829300-143829556 | Rare:111 | ||||
| chr8:143939540-143939748 | Common:3; Rare:66 | ||||
| chr8:143950856-143950974 | Common:1; Rare:41 | ||||
| chr8:143953778-143953942 | Common:3; Rare:50 | ||||
| chr8:143986406-143986478 | Rare:10 | ||||
| chr8:143989951-143990162 | Common:1; Rare:76 | ||||
| chr8:144060674-144060860 | Rare:58 | ||||
| chr8:144078532-144078722 | Common:1; Rare:57 | ||||
| chr8:144082503-144082701 | Common:2; Rare:67 | ||||
| chr8:144096214-144096367 | Common:1; Rare:59; Clinvar (benign):3 | ||||
| chr8:144103682-144103881 | Common:1; Rare:71 | ||||
| chr8:144104135-144104534 | Common:4; Rare:140 | ||||
| chr8:144137614-144137720 | Common:1; Rare:27 |