| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15427912-15428067 | Rare:20 | ||||
| chr4:15469591-15469923 | Common:1; Rare:67 | ||||
| chr4:15478892-15479307 | Common:2; Rare:94 | ||||
| chr4:15655289-15655473 | Common:1; Rare:83 | ||||
| chr4:15659824-15660083 | Common:1; Rare:51 | ||||
| chr4:15681458-15681869 | Common:3; Rare:142 | ||||
| chr4:16898404-16898462 | Rare:14 | ||||
| chr4:17614572-17614651 | Common:2; Rare:36 | ||||
| chr4:17810636-17811086 | Common:4; Rare:140 | ||||
| chr4:20254110-20254239 | Common:1; Rare:26 | ||||
| chr4:25160382-25160727 | Common:3; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914051-25914335 | Common:2; Rare:122 | ||||
| chr4:26320743-26321057 | Rare:132; Clinvar (benign):1 | ||||
| chr4:26860606-26860784 | Rare:55 | ||||
| chr4:30719966-30720105 | Common:1; Rare:27 |