| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:183124303-183124460 | Rare:59 | ||||
| chr2:185738684-185738910 | Common:2; Rare:83 | ||||
| chr2:185739055-185739212 | Rare:34 | ||||
| chr2:185745254-185745548 | Common:2; Rare:77 | ||||
| chr2:186485954-186486376 | Common:3; Rare:120 | ||||
| chr2:186589364-186589698 | Common:1; Rare:57 | ||||
| chr2:186589754-186589795 | Rare:8 | ||||
| chr2:186589932-186590491 | Rare:180 | ||||
| chr2:186849108-186849305 | Common:5; Rare:60 | ||||
| chr2:188291573-188292054 | Common:6; Rare:138 | ||||
| chr2:188292692-188292861 | Common:1; Rare:42 | ||||
| chr2:188292886-188293064 | Rare:27 | ||||
| chr2:189441030-189441519 | Common:3; Rare:156 | ||||
| chr2:189580736-189580896 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189661339-189661601 | Common:4; Rare:83 |