| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74958616-74958678 | Common:1; Rare:30 | ||||
| chr2:74958876-74959073 | Rare:70 | ||||
| chr2:75199513-75199622 | Rare:21 | ||||
| chr2:75710627-75710758 | Common:1; Rare:53 | ||||
| chr2:77593184-77593447 | Common:8; Rare:80 | ||||
| chr2:84459226-84459581 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905494-84906099 | Common:3; Rare:173 | ||||
| chr2:85327936-85328059 | Common:1; Rare:58 | ||||
| chr2:85354526-85354792 | Common:1; Rare:85 | ||||
| chr2:85413999-85414098 | Common:1; Rare:22 | ||||
| chr2:85539047-85539177 | Common:1; Rare:52 | ||||
| chr2:85561431-85561572 | Rare:52; Clinvar:4 | ||||
| chr2:85577409-85577632 | Common:2; Rare:54 | ||||
| chr2:85595491-85595826 | Common:3; Rare:112 | ||||
| chr2:85602667-85602853 | Rare:48 |