| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200811338-200811610 | Common:1; Rare:90 | ||||
| chr2:200864229-200864260 | Rare:10 | ||||
| chr2:200864606-200864788 | Common:1; Rare:71 | ||||
| chr2:200888974-200889445 | Common:3; Rare:149 | ||||
| chr2:200963630-200963915 | Common:1; Rare:71 | ||||
| chr2:201071617-201072049 | Rare:91 | ||||
| chr2:201116056-201116369 | Common:2; Rare:55 | ||||
| chr2:201118620-201118792 | Rare:26 | ||||
| chr2:201183022-201183147 | Common:1; Rare:17; Clinvar (benign):2 | ||||
| chr2:201257975-201258110 | Common:1; Rare:22 | ||||
| chr2:201451548-201451832 | Common:2; Rare:76 | ||||
| chr2:201642641-201642736 | Rare:49 | ||||
| chr2:201643438-201643648 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:202238498-202238640 | Rare:48 | ||||
| chr2:202265655-202265815 | Rare:63 |