| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:75630458-75630692 | Rare:55 | ||||
| chr4:75673049-75673216 | Rare:44 | ||||
| chr4:75673286-75673710 | Common:1; Rare:165 | ||||
| chr4:75724353-75724835 | Common:2; Rare:142 | ||||
| chr4:75990892-75990970 | Rare:32 | ||||
| chr4:76147833-76147955 | Common:2; Rare:29 | ||||
| chr4:76148356-76148597 | Common:4; Rare:75 | ||||
| chr4:76949549-76949889 | Common:2; Rare:114 | ||||
| chr4:77075967-77076105 | Common:3; Rare:70 | ||||
| chr4:77076278-77076490 | Common:3; Rare:96 | ||||
| chr4:77862635-77862879 | Common:3; Rare:90 | ||||
| chr4:78057234-78057404 | Common:2; Rare:41 | ||||
| chr4:78057494-78057605 | Common:2; Rare:23 | ||||
| chr4:78939239-78939608 | Common:2; Rare:153 | ||||
| chr4:80072588-80072909 | Common:3; Rare:88; Clinvar (benign):3 |