| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:182426702-182426852 | Rare:27 | ||||
| chr2:182867163-182867195 | Rare:9 | ||||
| chr2:183037996-183038212 | Rare:61 | ||||
| chr2:186485987-186486424 | Common:3; Rare:127 | ||||
| chr2:186589894-186590034 | Rare:40 | ||||
| chr2:186590061-186590073 | Rare:6 | ||||
| chr2:186590141-186590437 | Rare:99 | ||||
| chr2:188291672-188292047 | Common:4; Rare:102 | ||||
| chr2:189441133-189441511 | Common:2; Rare:116 | ||||
| chr2:189580736-189580957 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189661272-189661555 | Common:4; Rare:99 | ||||
| chr2:189783921-189784083 | Common:4; Rare:50; Clinvar (benign):1 | ||||
| chr2:189784282-189784537 | Common:4; Rare:92; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343856-190343960 | Rare:21 | ||||
| chr2:190343961-190344031 | Rare:14 |