| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55519409-55519913 | Common:2; Rare:165 | ||||
| chr2:55693821-55693983 | Common:1; Rare:49; Clinvar (benign):2 | ||||
| chr2:60550400-60550560 | Rare:31 | ||||
| chr2:60550881-60551011 | Rare:33 | ||||
| chr2:60553615-60553928 | Rare:47 | ||||
| chr2:60756170-60756338 | Rare:58 | ||||
| chr2:60881309-60881624 | Common:2; Rare:126 | ||||
| chr2:61017195-61017756 | Common:4; Rare:163; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61065732-61065961 | Common:1; Rare:77 | ||||
| chr2:61144921-61145164 | Common:3; Rare:82 | ||||
| chr2:61470667-61471032 | Common:1; Rare:119 | ||||
| chr2:61471257-61471386 | Common:2; Rare:46 | ||||
| chr2:61853988-61854097 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888499-61888700 | Common:1; Rare:87 | ||||
| chr2:62506141-62506227 | Rare:42 |