| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:149587109-149587476 | Common:4; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:149587685-149587882 | Common:1; Rare:57; Clinvar:1 | ||||
| chr2:151289611-151289704 | Common:1; Rare:26 | ||||
| chr2:151828336-151828638 | Common:3; Rare:96 | ||||
| chr2:152175685-152176079 | Common:2; Rare:109 | ||||
| chr2:152717829-152717947 | Rare:47 | ||||
| chr2:152717968-152718056 | Rare:27 | ||||
| chr2:152718458-152718702 | Rare:103 | ||||
| chr2:156332704-156332870 | Rare:49; Clinvar:2 | ||||
| chr2:157257808-157257917 | Rare:13 | ||||
| chr2:158968458-158968715 | Rare:82 | ||||
| chr2:159286613-159286893 | Common:5; Rare:101 | ||||
| chr2:159516535-159516665 | Common:1; Rare:15 | ||||
| chr2:159615225-159615343 | Common:2; Rare:28 | ||||
| chr2:159615418-159615696 | Common:2; Rare:87 |