| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218782026-218782183 | Rare:33; Clinvar (benign):1 | ||||
| chr2:219176903-219177035 | Common:3; Rare:40 | ||||
| chr2:219178149-219178424 | Common:6; Rare:119 | ||||
| chr2:219206688-219206923 | Rare:85 | ||||
| chr2:219229348-219229416 | Rare:23 | ||||
| chr2:219229582-219229896 | Common:2; Rare:91 | ||||
| chr2:219245401-219245531 | Rare:36 | ||||
| chr2:219253889-219254056 | Common:1; Rare:53 | ||||
| chr2:219279190-219279545 | Common:3; Rare:108; Clinvar (benign):1 | ||||
| chr2:219387790-219387939 | Rare:50 | ||||
| chr2:219498690-219498917 | Common:2; Rare:45 | ||||
| chr2:219597733-219597884 | Common:1; Rare:52 | ||||
| chr2:223052100-223052193 | Rare:19 | ||||
| chr2:223957306-223957470 | Common:3; Rare:66 | ||||
| chr2:226799165-226799346 | Common:1; Rare:40 |