| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139341738-139341994 | Common:1; Rare:71 | ||||
| chr5:139404016-139404192 | Rare:60 | ||||
| chr5:139439453-139439648 | Common:2; Rare:52 | ||||
| chr5:139561088-139561566 | Common:1; Rare:197 | ||||
| chr5:139561732-139561812 | Rare:30 | ||||
| chr5:140175014-140175275 | Common:1; Rare:64 | ||||
| chr5:140303048-140303187 | Common:1; Rare:45 | ||||
| chr5:140401393-140401883 | Common:3; Rare:102 | ||||
| chr5:140557397-140557578 | Common:3; Rare:107 | ||||
| chr5:140564317-140564470 | Common:1; Rare:44 | ||||
| chr5:140564573-140564858 | Rare:77 | ||||
| chr5:140639164-140639478 | Common:3; Rare:69 | ||||
| chr5:140647562-140647924 | Common:5; Rare:148; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664742-140664926 | Common:3; Rare:52 | ||||
| chr5:140691290-140691674 | Common:1; Rare:139; Clinvar:12; Clinvar (benign):2 |