| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201258277-201258379 | Rare:40 | ||||
| chr2:201451447-201451838 | Common:2; Rare:101 | ||||
| chr2:201625796-201626055 | Rare:59; Clinvar (benign):1 | ||||
| chr2:201642607-201642854 | Common:1; Rare:101; Clinvar (benign):1 | ||||
| chr2:201780867-201780984 | Common:2; Rare:33; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:202238524-202238615 | Rare:28 | ||||
| chr2:202265655-202265989 | Common:1; Rare:122 | ||||
| chr2:202871435-202871521 | Common:1; Rare:29 | ||||
| chr2:202911607-202912303 | Common:3; Rare:171 | ||||
| chr2:203238869-203239048 | Common:1; Rare:70 | ||||
| chr2:203328167-203328456 | Common:2; Rare:107 | ||||
| chr2:203328539-203328630 | Rare:20 | ||||
| chr2:203533386-203533490 | Rare:21 | ||||
| chr2:203535254-203535263 | Rare:1 | ||||
| chr2:205682353-205682591 | Rare:41 |