| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177264646-177264930 | Common:2; Rare:86 | ||||
| chr2:177552761-177552828 | Rare:27 | ||||
| chr2:178450735-178450897 | Rare:54 | ||||
| chr2:178451105-178451296 | Common:4; Rare:61; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:178478527-178478680 | Common:1; Rare:50 | ||||
| chr2:179861203-179861478 | Rare:89 | ||||
| chr2:181457232-181457417 | Rare:63 | ||||
| chr2:182715930-182716446 | Common:3; Rare:168 | ||||
| chr2:183124190-183124460 | Common:4; Rare:84 | ||||
| chr2:186485977-186486344 | Common:3; Rare:100 | ||||
| chr2:189783921-189784125 | Common:4; Rare:71; Clinvar (benign):1 | ||||
| chr2:189784305-189784537 | Common:4; Rare:84; Clinvar:7; Clinvar (benign):2 | ||||
| chr2:190319745-190319967 | Common:5; Rare:78; Clinvar (benign):5 | ||||
| chr2:190534681-190534882 | Common:1; Rare:66 | ||||
| chr2:190880604-190880826 | Common:3; Rare:65 |