| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177212428-177212832 | Common:4; Rare:160 | ||||
| chr2:177263402-177263709 | Common:1; Rare:76 | ||||
| chr2:177264534-177264705 | Common:1; Rare:52 | ||||
| chr2:177392672-177392814 | Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:177552761-177552838 | Common:1; Rare:29 | ||||
| chr2:177618706-177618750 | Common:1; Rare:18 | ||||
| chr2:178194382-178194651 | Common:2; Rare:73 | ||||
| chr2:178450731-178450892 | Rare:54 | ||||
| chr2:178451083-178451325 | Common:5; Rare:73; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478534-178478659 | Common:1; Rare:35 | ||||
| chr2:180980828-180980964 | Rare:31 | ||||
| chr2:181457237-181457410 | Rare:58 | ||||
| chr2:182716112-182716406 | Common:2; Rare:97 | ||||
| chr2:183038001-183038207 | Rare:60 | ||||
| chr2:186485966-186486376 | Common:3; Rare:117 |