| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:148020688-148021114 | Common:2; Rare:98; Clinvar (benign):2 | ||||
| chr2:148021533-148021679 | Rare:29; Clinvar (benign):1 | ||||
| chr2:149587295-149587385 | Common:1; Rare:21 | ||||
| chr2:149587662-149587823 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:152175823-152176172 | Common:1; Rare:90 | ||||
| chr2:152659166-152659281 | Common:1; Rare:39 | ||||
| chr2:152717831-152718050 | Rare:85 | ||||
| chr2:152718494-152718639 | Rare:54 | ||||
| chr2:152718801-152718859 | Rare:35; Clinvar:1 | ||||
| chr2:157257804-157258120 | Common:1; Rare:57 | ||||
| chr2:158456727-158456952 | Common:1; Rare:74 | ||||
| chr2:159615218-159615324 | Common:2; Rare:22 | ||||
| chr2:159615551-159615692 | Common:1; Rare:47 | ||||
| chr2:159712334-159712603 | Common:2; Rare:98 | ||||
| chr2:162073301-162073345 | Rare:5 |