| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73931540-73931596 | Common:2; Rare:10 | ||||
| chr2:73956897-73957176 | Rare:78; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr2:73984030-73984225 | Rare:42 | ||||
| chr2:73984898-73985031 | Common:1; Rare:50 | ||||
| chr2:74030830-74030945 | Common:1; Rare:18 | ||||
| chr2:74120211-74120402 | Common:1; Rare:66 | ||||
| chr2:74211815-74211935 | Rare:28 | ||||
| chr2:74370177-74370828 | Common:2; Rare:167; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74377447-74377669 | Common:1; Rare:58 | ||||
| chr2:74387588-74387756 | Common:1; Rare:24 | ||||
| chr2:74503940-74504441 | Common:2; Rare:95 | ||||
| chr2:74557494-74557608 | Common:1; Rare:21 | ||||
| chr2:75272785-75272944 | Rare:34 | ||||
| chr2:75506464-75506556 | Common:2; Rare:12 | ||||
| chr2:75525273-75525364 | Common:1; Rare:20 |