| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189661286-189661528 | Common:4; Rare:93 | ||||
| chr2:189674375-189674727 | Common:2; Rare:82 | ||||
| chr2:189783965-189784089 | Common:3; Rare:45; Clinvar (benign):1 | ||||
| chr2:189784281-189784512 | Common:3; Rare:76; Clinvar:7; Clinvar (benign):1 | ||||
| chr2:190534688-190534862 | Common:1; Rare:57 | ||||
| chr2:190880637-190880829 | Common:3; Rare:59 | ||||
| chr2:191014139-191014333 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245283-191245570 | Common:2; Rare:92 | ||||
| chr2:191246162-191246289 | Rare:38 | ||||
| chr2:191677858-191678161 | Common:4; Rare:85 | ||||
| chr2:196068778-196068933 | Common:1; Rare:49 | ||||
| chr2:197434986-197435198 | Rare:70 | ||||
| chr2:197499815-197500424 | Common:1; Rare:236; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515792-197516087 | Common:2; Rare:106 | ||||
| chr2:197705189-197705390 | Common:3; Rare:80 |