| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169010237-169010474 | Common:1; Rare:72 | ||||
| chr4:169612562-169612797 | Common:4; Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:169620415-169620725 | Common:2; Rare:105 | ||||
| chr4:169757842-169758074 | Common:1; Rare:72 | ||||
| chr4:170026305-170026599 | Common:4; Rare:113 | ||||
| chr4:170027294-170027405 | Common:1; Rare:30 | ||||
| chr4:170089294-170089595 | Common:1; Rare:77 | ||||
| chr4:170089769-170090087 | Common:2; Rare:86 | ||||
| chr4:171812153-171812394 | Rare:51 | ||||
| chr4:171812632-171812742 | Common:2; Rare:21 | ||||
| chr4:171813292-171813448 | Common:1; Rare:51 | ||||
| chr4:173369754-173369935 | Common:1; Rare:63 | ||||
| chr4:173370668-173370961 | Common:2; Rare:72 | ||||
| chr4:174283163-174283353 | Rare:28 | ||||
| chr4:174283612-174284032 | Common:1; Rare:94 |