| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:159615188-159615343 | Common:3; Rare:32 | ||||
| chr2:159711956-159712275 | Common:2; Rare:85 | ||||
| chr2:159712334-159712603 | Common:2; Rare:98 | ||||
| chr2:159904706-159904869 | Rare:39 | ||||
| chr2:161308376-161308579 | Common:2; Rare:48 | ||||
| chr2:161624040-161624548 | Common:1; Rare:91 | ||||
| chr2:162838591-162838798 | Rare:53 | ||||
| chr2:163735871-163736159 | Common:1; Rare:50 | ||||
| chr2:164840467-164840760 | Common:1; Rare:52 | ||||
| chr2:164841821-164841906 | Common:1; Rare:24 | ||||
| chr2:164955476-164955566 | Rare:21 | ||||
| chr2:165469534-165469722 | Rare:36 | ||||
| chr2:165572240-165572431 | Rare:31 | ||||
| chr2:165574118-165574357 | Rare:46 | ||||
| chr2:165953723-165954095 | Common:3; Rare:128; Clinvar:6; Clinvar (benign):2 |