| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:76148326-76148601 | Common:4; Rare:83 | ||||
| chr4:76213429-76213500 | Common:1; Rare:20; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:76213513-76214023 | Common:4; Rare:178; Clinvar:1; Clinvar (benign):6 | ||||
| chr4:76949618-76949921 | Common:1; Rare:93 | ||||
| chr4:76987729-76987769 | Rare:7 | ||||
| chr4:76988129-76988341 | Rare:35 | ||||
| chr4:77055984-77056296 | Common:3; Rare:70 | ||||
| chr4:77075473-77075649 | Common:1; Rare:82 | ||||
| chr4:77075918-77076161 | Common:4; Rare:114 | ||||
| chr4:77076271-77076403 | Common:3; Rare:68 | ||||
| chr4:77158326-77158588 | Common:1; Rare:91 | ||||
| chr4:77862653-77862911 | Common:3; Rare:108 | ||||
| chr4:78939348-78939533 | Common:2; Rare:91 | ||||
| chr4:80073034-80073252 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:80073470-80073646 | Common:2; Rare:42 |