| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:63841618-63841921 | Common:2; Rare:102 | ||||
| chr2:64524115-64524438 | Common:3; Rare:102 | ||||
| chr2:64653894-64654071 | Common:1; Rare:59 | ||||
| chr2:65056186-65056462 | Common:2; Rare:95 | ||||
| chr2:65227579-65227946 | Rare:100 | ||||
| chr2:66434811-66435171 | Common:1; Rare:87 | ||||
| chr2:68157477-68157966 | Common:3; Rare:254 | ||||
| chr2:68467275-68467642 | Common:1; Rare:102 | ||||
| chr2:68774718-68775007 | Common:1; Rare:60 | ||||
| chr2:69387106-69387406 | Common:1; Rare:84; Clinvar:2 | ||||
| chr2:69643605-69643829 | Rare:79 | ||||
| chr2:70293659-70293902 | Common:3; Rare:78 | ||||
| chr2:71068545-71068678 | Rare:56 | ||||
| chr2:71130225-71130677 | Common:6; Rare:129; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71453437-71453500 | Rare:11 |