| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61017357-61017763 | Common:1; Rare:128; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61018148-61018221 | Rare:21 | ||||
| chr2:61018231-61018363 | Rare:46 | ||||
| chr2:61065678-61066014 | Common:3; Rare:110 | ||||
| chr2:61066521-61066604 | Common:1; Rare:22 | ||||
| chr2:61066606-61066636 | Rare:5 | ||||
| chr2:61144868-61145182 | Common:3; Rare:103 | ||||
| chr2:61176909-61177579 | Common:8; Rare:242 | ||||
| chr2:61178014-61178144 | Rare:41 | ||||
| chr2:61178304-61178331 | Rare:7 | ||||
| chr2:61470618-61471494 | Common:5; Rare:304 | ||||
| chr2:61536584-61536902 | Common:1; Rare:101 | ||||
| chr2:61538124-61538464 | Common:1; Rare:87 | ||||
| chr2:61538674-61538994 | Common:1; Rare:95 | ||||
| chr2:61853734-61853823 | Rare:21 |