| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203239201-203239349 | Rare:50 | ||||
| chr2:203328190-203328444 | Common:2; Rare:96 | ||||
| chr2:203535139-203535546 | Common:3; Rare:154 | ||||
| chr2:206085765-206085963 | Common:1; Rare:57 | ||||
| chr2:206159346-206160059 | Common:4; Rare:214; Clinvar (benign):1 | ||||
| chr2:206765284-206765654 | Common:3; Rare:103; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207529818-207530111 | Common:1; Rare:82 | ||||
| chr2:207625183-207625506 | Common:1; Rare:93 | ||||
| chr2:208253884-208254231 | Common:1; Rare:61 | ||||
| chr2:208254431-208254590 | Common:1; Rare:33 | ||||
| chr2:208254942-208255234 | Common:2; Rare:71 | ||||
| chr2:208266032-208266303 | Common:9; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210671368-210671599 | Common:2; Rare:43 | ||||
| chr2:213284172-213284499 | Rare:102 | ||||
| chr2:215312018-215312152 | Common:7; Rare:64 |