| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:86199366-86199506 | Common:2; Rare:88 | ||||
| chr2:86337570-86337780 | Rare:64 | ||||
| chr2:86440630-86440970 | Common:6; Rare:213 | ||||
| chr2:86441141-86441500 | Common:2; Rare:138 | ||||
| chr2:86563310-86563561 | Common:4; Rare:157 | ||||
| chr2:86622830-86623540 | Common:3; Rare:224 | ||||
| chr2:86623803-86624010 | Common:3; Rare:181 | ||||
| chr2:86719810-86720110 | Rare:77 | ||||
| chr2:86720264-86720448 | Rare:76 | ||||
| chr2:88055240-88055650 | Rare:194 | ||||
| chr2:88055696-88055930 | Rare:157 | ||||
| chr2:88627356-88627922 | Common:3; Rare:159; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:88691360-88691853 | Common:6; Rare:339; Clinvar:2 | ||||
| chr2:95121710-95122089 | Common:1; Rare:214 | ||||
| chr2:95159490-95159921 | Common:11; Rare:322 |