| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74958534-74958682 | Common:3; Rare:52 | ||||
| chr2:74958876-74959032 | Rare:59 | ||||
| chr2:75710630-75710787 | Common:2; Rare:63 | ||||
| chr2:75710872-75711042 | Common:1; Rare:57 | ||||
| chr2:84459177-84459581 | Common:3; Rare:110; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905470-84905949 | Common:2; Rare:143 | ||||
| chr2:85327916-85328066 | Common:1; Rare:68 | ||||
| chr2:85328268-85328307 | Rare:8 | ||||
| chr2:85354517-85354807 | Common:1; Rare:98 | ||||
| chr2:85539072-85539170 | Common:1; Rare:37 | ||||
| chr2:85561424-85561571 | Rare:53; Clinvar:4 | ||||
| chr2:85577548-85577623 | Common:1; Rare:21 | ||||
| chr2:85595555-85595788 | Common:2; Rare:79 | ||||
| chr2:85602657-85602900 | Rare:59 | ||||
| chr2:85612007-85612138 | Rare:42 |