| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135769446-135769792 | Common:1; Rare:59 | ||||
| chr2:143070766-143071023 | Common:1; Rare:55 | ||||
| chr2:156293082-156293116 | Common:1; Rare:11 | ||||
| chr2:159765134-159765248 | Common:3; Rare:18 | ||||
| chr2:159780089-159780412 | Common:1; Rare:86 | ||||
| chr2:159780952-159781116 | Common:2; Rare:47 | ||||
| chr2:161339833-161339884 | Rare:3 | ||||
| chr2:161339887-161340146 | Common:1; Rare:31 | ||||
| chr2:177234244-177234360 | Rare:31 | ||||
| chr2:182866079-182866103 | Rare:10 | ||||
| chr2:182866168-182866308 | Rare:52; Clinvar:1 | ||||
| chr2:182866331-182866442 | Rare:35 | ||||
| chr2:189006833-189006968 | Common:3; Rare:40; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
| chr2:190950546-190950755 | Common:2; Rare:42 | ||||
| chr2:202375736-202375863 | Rare:30 |