| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38076138-38076291 | Rare:38 | ||||
| chr2:38602895-38603187 | Common:4; Rare:114 | ||||
| chr2:38875886-38876065 | Common:1; Rare:66 | ||||
| chr2:39437078-39437456 | Common:4; Rare:136 | ||||
| chr2:40511701-40512027 | Common:1; Rare:62 | ||||
| chr2:40610928-40611003 | Common:1; Rare:17 | ||||
| chr2:42169164-42169387 | Common:1; Rare:115 | ||||
| chr2:44361479-44361987 | Common:3; Rare:160 | ||||
| chr2:46297675-46297799 | Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46617019-46617262 | Common:7; Rare:106 | ||||
| chr2:46699079-46699358 | Common:1; Rare:84 | ||||
| chr2:46915722-46916094 | Common:4; Rare:121; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176430-47176847 | Common:4; Rare:191; Clinvar (benign):5 | ||||
| chr2:47402925-47403180 | Common:1; Rare:114; Clinvar:36; Clinvar (benign):23 | ||||
| chr2:48440631-48440815 | Common:5; Rare:79 |