| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200854679-200854817 | Rare:41 | ||||
| chr2:200855001-200855005 | |||||
| chr2:200864198-200864260 | Rare:23 | ||||
| chr2:200864552-200864788 | Common:1; Rare:85 | ||||
| chr2:200888568-200888866 | Rare:69 | ||||
| chr2:200888989-200889568 | Common:4; Rare:168 | ||||
| chr2:200963499-200963884 | Common:1; Rare:100 | ||||
| chr2:201071570-201072052 | Rare:109 | ||||
| chr2:201115941-201116438 | Common:2; Rare:90 | ||||
| chr2:201117346-201117604 | Rare:32 | ||||
| chr2:201118543-201118798 | Rare:40 | ||||
| chr2:201258073-201258244 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chr2:201258290-201258404 | Rare:46 | ||||
| chr2:201451416-201451816 | Common:2; Rare:108 | ||||
| chr2:201473220-201473397 | Rare:23 |