| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74835128-74835316 | Rare:47 | ||||
| chr2:74958603-74959091 | Common:4; Rare:198 | ||||
| chr2:75560827-75561114 | Common:1; Rare:72 | ||||
| chr2:75561250-75561380 | Common:1; Rare:16 | ||||
| chr2:75710601-75710808 | Common:2; Rare:86 | ||||
| chr2:75710862-75711103 | Common:1; Rare:79 | ||||
| chr2:84459172-84459572 | Common:3; Rare:110; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905021-84905366 | Common:2; Rare:72 | ||||
| chr2:84905482-84906124 | Common:3; Rare:183 | ||||
| chr2:84970666-84970815 | Common:1; Rare:42 | ||||
| chr2:84970920-84971454 | Common:3; Rare:155 | ||||
| chr2:85327933-85328327 | Common:7; Rare:129 | ||||
| chr2:85354550-85354790 | Common:1; Rare:72 | ||||
| chr2:85539055-85539373 | Common:3; Rare:153; Clinvar (benign):7 | ||||
| chr2:85540857-85541015 | Rare:29 |