| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:152717829-152717924 | Rare:41 | ||||
| chr2:152717991-152718296 | Common:1; Rare:98 | ||||
| chr2:152718405-152718643 | Common:2; Rare:87 | ||||
| chr2:156436264-156436459 | Common:3; Rare:63 | ||||
| chr2:159712404-159712575 | Common:2; Rare:70 | ||||
| chr2:162243385-162243624 | Common:1; Rare:42 | ||||
| chr2:165953809-165953978 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:171433991-171434224 | Common:1; Rare:63 | ||||
| chr2:171522262-171522523 | Common:3; Rare:61 | ||||
| chr2:173354586-173354901 | Common:1; Rare:94 | ||||
| chr2:174248461-174248744 | Common:1; Rare:85 | ||||
| chr2:174395650-174395784 | Common:1; Rare:44 | ||||
| chr2:174487061-174487390 | Common:2; Rare:73 | ||||
| chr2:176002237-176002398 | Common:2; Rare:65 | ||||
| chr2:177212432-177212771 | Common:4; Rare:135 |