| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:84459210-84459572 | Common:3; Rare:93; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905537-84905940 | Common:1; Rare:117 | ||||
| chr2:84906996-84907298 | Common:1; Rare:55 | ||||
| chr2:85354501-85354790 | Common:1; Rare:97 | ||||
| chr2:85539024-85539172 | Common:1; Rare:60 | ||||
| chr2:85561425-85561571 | Rare:53; Clinvar:4 | ||||
| chr2:85595558-85595847 | Common:1; Rare:101 | ||||
| chr2:85602629-85602904 | Rare:72 | ||||
| chr2:85611993-85612113 | Rare:48 | ||||
| chr2:85753447-85753935 | Common:3; Rare:128 | ||||
| chr2:85754077-85754151 | Rare:15 | ||||
| chr2:85888831-85889131 | Common:3; Rare:93; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:86105843-86106257 | Common:3; Rare:115 | ||||
| chr2:86195387-86195530 | Common:4; Rare:50 | ||||
| chr2:86441175-86441497 | Common:2; Rare:123 |