| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:169798767-169798970 | Rare:53 | ||||
| chr2:170928927-170929239 | Common:4; Rare:77 | ||||
| chr2:171433991-171434224 | Common:1; Rare:63 | ||||
| chr2:171999837-171999964 | Common:1; Rare:55 | ||||
| chr2:172084619-172084749 | Rare:35 | ||||
| chr2:174248465-174248751 | Common:1; Rare:87 | ||||
| chr2:174395670-174395808 | Common:1; Rare:41 | ||||
| chr2:176002235-176002389 | Common:2; Rare:66 | ||||
| chr2:177212434-177212797 | Common:4; Rare:148 | ||||
| chr2:177392672-177392801 | Rare:33; Clinvar:1 | ||||
| chr2:178451095-178451363 | Common:5; Rare:79; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:183124252-183124466 | Common:4; Rare:73 | ||||
| chr2:186486037-186486344 | Common:3; Rare:86 | ||||
| chr2:189441138-189441497 | Common:2; Rare:103 | ||||
| chr2:189783991-189784078 | Rare:26 |