| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74554678-74554755 | Common:1; Rare:33 | ||||
| chr2:74555624-74555802 | Common:1; Rare:51 | ||||
| chr2:74654112-74654280 | Rare:42 | ||||
| chr2:74958876-74959011 | Rare:53 | ||||
| chr2:75518610-75518851 | Common:2; Rare:45 | ||||
| chr2:75646942-75647182 | Common:2; Rare:64 | ||||
| chr2:75710630-75710802 | Common:2; Rare:74 | ||||
| chr2:75710872-75711098 | Common:1; Rare:71 | ||||
| chr2:84459219-84459593 | Common:3; Rare:95; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905510-84905910 | Common:1; Rare:119 | ||||
| chr2:85327741-85328097 | Common:7; Rare:127 | ||||
| chr2:85354501-85354807 | Common:1; Rare:105 | ||||
| chr2:85538893-85539178 | Common:2; Rare:97 | ||||
| chr2:85560948-85561018 | Common:1; Rare:24 | ||||
| chr2:85561394-85561606 | Rare:75; Clinvar:5 |