| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:93591810-93592047 | Common:1; Rare:33 | ||||
| chr5:94618529-94618696 | Rare:44 | ||||
| chr5:95495727-95495862 | Rare:22 | ||||
| chr5:95512865-95513164 | Common:1; Rare:53 | ||||
| chr5:95516380-95516682 | Common:2; Rare:96; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:95554925-95555216 | Common:1; Rare:80 | ||||
| chr5:95731000-95731391 | Rare:121 | ||||
| chr5:95783636-95783960 | Common:1; Rare:78 | ||||
| chr5:95822435-95822950 | Rare:136 | ||||
| chr5:95900772-95901080 | Rare:68 | ||||
| chr5:95961572-95962012 | Common:1; Rare:136 | ||||
| chr5:96661971-96662080 | Common:1; Rare:20 | ||||
| chr5:96662181-96662493 | Common:1; Rare:111 | ||||
| chr5:96662860-96663087 | Common:1; Rare:52 | ||||
| chr5:96702553-96702916 | Common:1; Rare:87 |