| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191677856-191678146 | Common:4; Rare:81 | ||||
| chr2:197434996-197435297 | Rare:94 | ||||
| chr2:197499815-197500416 | Common:1; Rare:233; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:200889037-200889424 | Common:2; Rare:126 | ||||
| chr2:201071637-201072048 | Rare:84 | ||||
| chr2:201642668-201642744 | Rare:39 | ||||
| chr2:202912125-202912286 | Common:2; Rare:54 | ||||
| chr2:206085772-206085883 | Rare:34 | ||||
| chr2:206159414-206159681 | Rare:88 | ||||
| chr2:206274938-206275034 | Rare:38 | ||||
| chr2:206765297-206765639 | Common:3; Rare:84; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:207165937-207166142 | Rare:39 | ||||
| chr2:207529788-207530104 | Common:2; Rare:89 | ||||
| chr2:207625256-207625553 | Common:1; Rare:85 | ||||
| chr2:208255047-208255238 | Common:2; Rare:51 |