| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:156949950-156950470 | Common:16; Rare:392 | ||||
| chr7:157009250-157009651 | Common:1; Rare:157 | ||||
| chr7:157010616-157010869 | Common:9; Rare:160 | ||||
| chr7:157138633-157139001 | Common:4; Rare:120 | ||||
| chr7:158587626-158588131 | Common:10; Rare:189 | ||||
| chr7:158704733-158704995 | Common:2; Rare:168 | ||||
| chr7:158829417-158829723 | Common:7; Rare:210 | ||||
| chr7:158856362-158856699 | Common:13; Rare:189 | ||||
| chr8:232152-232462 | Common:5; Rare:214 | ||||
| chr8:406828-407033 | Rare:158 | ||||
| chr8:545370-545710 | Common:6; Rare:254 | ||||
| chr8:731151-731394 | Common:6; Rare:180 | ||||
| chr8:1755562-1755824 | Common:6; Rare:143 | ||||
| chr8:1763188-1764499 | Common:51; Rare:601; Clinvar:3; Clinvar (benign):6 | ||||
| chr8:6406412-6406709 | Common:11; Rare:241; Clinvar:4; Clinvar (benign):2 |