| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39124313-39124569 | Common:1; Rare:90 | ||||
| chr2:39437065-39437486 | Common:4; Rare:151 | ||||
| chr2:40451602-40451814 | Common:4; Rare:66 | ||||
| chr2:42169086-42169604 | Common:3; Rare:217 | ||||
| chr2:42792732-42792978 | Common:1; Rare:63 | ||||
| chr2:43225741-43226061 | Common:3; Rare:122 | ||||
| chr2:43226232-43226426 | Common:1; Rare:84 | ||||
| chr2:43226600-43226875 | Common:2; Rare:106 | ||||
| chr2:43595940-43596197 | Common:1; Rare:90 | ||||
| chr2:43995960-43996289 | Common:4; Rare:143; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:44361131-44361151 | Rare:5 | ||||
| chr2:44361473-44362023 | Common:4; Rare:175 | ||||
| chr2:45567955-45568156 | Common:3; Rare:44 | ||||
| chr2:45651562-45651703 | Common:1; Rare:36 | ||||
| chr2:46297042-46297468 | Common:7; Rare:156; Clinvar:1; Clinvar (benign):1 |