| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:63588446-63589040 | Common:2; Rare:172; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:63840820-63841207 | Common:3; Rare:109 | ||||
| chr2:63841620-63841927 | Common:2; Rare:105 | ||||
| chr2:64144089-64144295 | Common:3; Rare:45 | ||||
| chr2:64144319-64144709 | Common:4; Rare:111 | ||||
| chr2:64454033-64454224 | Rare:40 | ||||
| chr2:64454585-64455103 | Rare:134 | ||||
| chr2:64524108-64524494 | Common:3; Rare:122 | ||||
| chr2:64653738-64654071 | Common:1; Rare:113 | ||||
| chr2:65056180-65056458 | Common:2; Rare:95 | ||||
| chr2:65227615-65227955 | Rare:92 | ||||
| chr2:66434828-66435175 | Common:1; Rare:80 | ||||
| chr2:67397298-67397545 | Rare:86 | ||||
| chr2:68157493-68157966 | Common:3; Rare:243 | ||||
| chr2:68252124-68252325 | Common:2; Rare:66 |