| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:179950648-179950852 | Common:3; Rare:58 | ||||
| chr2:181014039-181014232 | Common:2; Rare:35 | ||||
| chr2:186495313-186495567 | Rare:45 | ||||
| chr2:186649092-186649099 | |||||
| chr2:188978626-188978826 | Common:3; Rare:29 | ||||
| chr2:189004253-189004477 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):16 | ||||
| chr2:189473925-189474285 | Common:1; Rare:74 | ||||
| chr2:189475535-189475660 | Rare:24 | ||||
| chr2:189727592-189727707 | Rare:8 | ||||
| chr2:189855077-189855321 | Rare:45 | ||||
| chr2:190366610-190366734 | Common:1; Rare:26 | ||||
| chr2:190954161-190954403 | Common:2; Rare:39 | ||||
| chr2:196268495-196268760 | Common:6; Rare:55 | ||||
| chr2:196922410-196922575 | Rare:24 | ||||
| chr2:197486425-197486771 | Common:2; Rare:59; Clinvar:2 |