| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:205682356-205682563 | Rare:35 | ||||
| chr2:206085772-206085965 | Common:1; Rare:55 | ||||
| chr2:206159379-206160014 | Common:4; Rare:193; Clinvar (benign):1 | ||||
| chr2:206274928-206275052 | Common:1; Rare:45 | ||||
| chr2:206765284-206765654 | Common:3; Rare:103; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165925-207166142 | Rare:44 | ||||
| chr2:207529713-207530025 | Common:3; Rare:102 | ||||
| chr2:207625195-207625591 | Common:1; Rare:111 | ||||
| chr2:208025499-208025620 | Rare:30 | ||||
| chr2:208254231-208254527 | Rare:76 | ||||
| chr2:208255005-208255238 | Common:2; Rare:61 | ||||
| chr2:208266111-208266302 | Common:6; Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209423753-209424081 | Common:2; Rare:96 | ||||
| chr2:210476691-210476846 | Rare:42 | ||||
| chr2:210477539-210477707 | Rare:51 |