| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:36966451-36966876 | Common:4; Rare:186 | ||||
| chr2:37084258-37084559 | Common:4; Rare:109 | ||||
| chr2:37156899-37157129 | Common:1; Rare:76 | ||||
| chr2:37196412-37196776 | Common:5; Rare:123 | ||||
| chr2:37230828-37231128 | Common:2; Rare:61 | ||||
| chr2:37231264-37231370 | Common:1; Rare:43 | ||||
| chr2:37231466-37231788 | Common:6; Rare:175; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:37323801-37323945 | Common:3; Rare:41 | ||||
| chr2:37324000-37324267 | Common:1; Rare:69 | ||||
| chr2:37324383-37324989 | Common:3; Rare:199 | ||||
| chr2:37325055-37325175 | Rare:26 | ||||
| chr2:37344606-37344639 | Rare:15 | ||||
| chr2:37344655-37344727 | Common:1; Rare:28 | ||||
| chr2:37671616-37671723 | Common:1; Rare:57 | ||||
| chr2:37672181-37672434 | Common:4; Rare:68 |