| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216694723-216694854 | Rare:34 | ||||
| chr2:217885745-217886108 | Common:4; Rare:92 | ||||
| chr2:217905339-217905614 | Rare:58 | ||||
| chr2:217919920-217920177 | Common:5; Rare:57 | ||||
| chr2:217937475-217937726 | Rare:56 | ||||
| chr2:217978639-217978734 | Rare:29 | ||||
| chr2:217978770-217978956 | Common:1; Rare:59 | ||||
| chr2:218217058-218217246 | Common:1; Rare:67 | ||||
| chr2:218270091-218270573 | Common:5; Rare:155; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218287258-218287356 | Rare:17 | ||||
| chr2:218322986-218323259 | Common:5; Rare:86 | ||||
| chr2:218568290-218568598 | Common:2; Rare:84 | ||||
| chr2:218659334-218659738 | Common:4; Rare:95 | ||||
| chr2:218671977-218672339 | Common:2; Rare:89 | ||||
| chr2:219176897-219177109 | Common:4; Rare:64 |