| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157160069-157160343 | Rare:216 | ||||
| chr3:157160510-157160960 | Common:12; Rare:144 | ||||
| chr3:158110007-158110205 | Rare:48 | ||||
| chr3:158110220-158110477 | Common:3; Rare:87 | ||||
| chr3:158801997-158802169 | Common:4; Rare:148 | ||||
| chr3:160399157-160399338 | Rare:94; Clinvar:4 | ||||
| chr3:160399487-160399707 | Rare:104; Clinvar:2 | ||||
| chr3:160449733-160450075 | Common:4; Rare:210 | ||||
| chr3:160565292-160565836 | Common:4; Rare:256 | ||||
| chr3:160755442-160755664 | Common:1; Rare:83 | ||||
| chr3:160755914-160756277 | Common:2; Rare:172 | ||||
| chr3:161221216-161221438 | Common:5; Rare:118 | ||||
| chr3:161371487-161371774 | Common:4; Rare:97 | ||||
| chr3:167734827-167735243 | Common:7; Rare:258; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:167735571-167735752 | Rare:73 |