| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74958603-74959080 | Common:4; Rare:197 | ||||
| chr2:75710636-75710802 | Common:2; Rare:72 | ||||
| chr2:75710860-75711256 | Common:2; Rare:105 | ||||
| chr2:77593240-77593474 | Common:7; Rare:74 | ||||
| chr2:84459182-84459601 | Common:3; Rare:112; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84881075-84881406 | Common:2; Rare:81 | ||||
| chr2:84905580-84905738 | Common:1; Rare:46 | ||||
| chr2:84970670-84970821 | Common:1; Rare:43 | ||||
| chr2:84970920-84971449 | Common:3; Rare:155 | ||||
| chr2:85133152-85133468 | Common:1; Rare:97 | ||||
| chr2:85327916-85328105 | Common:3; Rare:86 | ||||
| chr2:85328224-85328305 | Common:2; Rare:18 | ||||
| chr2:85354501-85354854 | Common:2; Rare:115 | ||||
| chr2:85413601-85413723 | Rare:37 | ||||
| chr2:85413959-85414102 | Common:1; Rare:31 |