| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61177158-61177474 | Common:6; Rare:127 | ||||
| chr2:61470651-61470991 | Rare:112 | ||||
| chr2:61471078-61471399 | Common:4; Rare:124 | ||||
| chr2:61536710-61536816 | Rare:38 | ||||
| chr2:61537063-61537122 | Rare:13 | ||||
| chr2:61537965-61538122 | Common:2; Rare:28 | ||||
| chr2:61538181-61538382 | Common:1; Rare:48 | ||||
| chr2:61538503-61538810 | Common:1; Rare:76 | ||||
| chr2:61853963-61854121 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888379-61888748 | Common:2; Rare:163 | ||||
| chr2:62506125-62506297 | Common:1; Rare:70 | ||||
| chr2:62705560-62705736 | Rare:49 | ||||
| chr2:63588220-63588591 | Common:1; Rare:115; Clinvar:6 | ||||
| chr2:63588729-63589040 | Rare:96 | ||||
| chr2:63840813-63841171 | Common:2; Rare:102 |