| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219176874-219177109 | Common:4; Rare:71 | ||||
| chr2:219177811-219177917 | Common:4; Rare:20 | ||||
| chr2:219229553-219229912 | Common:2; Rare:113 | ||||
| chr2:219245414-219245539 | Common:1; Rare:37 | ||||
| chr2:219253874-219254056 | Common:1; Rare:57 | ||||
| chr2:219279139-219279506 | Common:2; Rare:112 | ||||
| chr2:219498667-219498929 | Common:2; Rare:56 | ||||
| chr2:219597684-219597901 | Common:1; Rare:83 | ||||
| chr2:223957248-223957505 | Common:4; Rare:101; Clinvar (benign):1 | ||||
| chr2:224946879-224947207 | Common:1; Rare:61 | ||||
| chr2:226836392-226836425 | Common:1; Rare:6 | ||||
| chr2:227325216-227325321 | Common:2; Rare:37 | ||||
| chr2:229271230-229271389 | Common:1; Rare:47 | ||||
| chr2:230225622-230225773 | Rare:32 | ||||
| chr2:230327067-230327234 | Rare:38 |