| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24971603-24972166 | Common:4; Rare:196 | ||||
| chr2:25041954-25042315 | Common:5; Rare:91 | ||||
| chr2:25878455-25878746 | Common:3; Rare:92 | ||||
| chr2:25982075-25982332 | Common:1; Rare:45 | ||||
| chr2:25982379-25982808 | Common:2; Rare:106 | ||||
| chr2:26033775-26034194 | Common:4; Rare:154 | ||||
| chr2:26034263-26034668 | Common:4; Rare:107 | ||||
| chr2:26244581-26244984 | Common:2; Rare:148; Clinvar:5; Clinvar (benign):9 | ||||
| chr2:26345773-26346235 | Common:1; Rare:143 | ||||
| chr2:26401830-26402035 | Common:4; Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:26764193-26764347 | Common:2; Rare:61 | ||||
| chr2:26847906-26848264 | Common:2; Rare:98 | ||||
| chr2:27032862-27032983 | Rare:44 | ||||
| chr2:27051535-27051748 | Rare:66 | ||||
| chr2:27071324-27071898 | Common:2; Rare:179 |