| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169612579-169612797 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:169620358-169620718 | Common:2; Rare:127 | ||||
| chr4:169660036-169660261 | Common:1; Rare:42 | ||||
| chr4:169757873-169758062 | Rare:56 | ||||
| chr4:173333502-173333867 | Common:2; Rare:94 | ||||
| chr4:173369802-173369935 | Common:1; Rare:45 | ||||
| chr4:173370693-173370976 | Common:2; Rare:71 | ||||
| chr4:173530127-173530487 | Common:2; Rare:75 | ||||
| chr4:174283111-174283332 | Rare:32 | ||||
| chr4:174283549-174283977 | Common:1; Rare:83 | ||||
| chr4:174522449-174522622 | Rare:55; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:176195563-176195711 | Common:1; Rare:56 | ||||
| chr4:176319721-176320028 | Common:4; Rare:102 | ||||
| chr4:177442376-177442530 | Rare:93; Clinvar:2 | ||||
| chr4:182917319-182917519 | Common:3; Rare:77 |