| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203238892-203239037 | Rare:56 | ||||
| chr2:203239220-203239322 | Rare:34 | ||||
| chr2:203328066-203328453 | Common:2; Rare:138 | ||||
| chr2:205682353-205682594 | Rare:42 | ||||
| chr2:206085765-206085965 | Common:1; Rare:57 | ||||
| chr2:206159378-206160058 | Common:4; Rare:209; Clinvar (benign):1 | ||||
| chr2:206274918-206275043 | Rare:46 | ||||
| chr2:206765293-206765661 | Common:3; Rare:98; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165928-207166092 | Rare:30 | ||||
| chr2:207529774-207530116 | Common:3; Rare:93 | ||||
| chr2:207625226-207625587 | Common:1; Rare:100 | ||||
| chr2:208254236-208254492 | Rare:65 | ||||
| chr2:208254946-208255244 | Common:2; Rare:73 | ||||
| chr2:208266032-208266313 | Common:9; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209423788-209424132 | Common:1; Rare:103 |