| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218270107-218270532 | Common:5; Rare:127; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218316642-218316783 | Common:1; Rare:13 | ||||
| chr2:218322986-218323264 | Common:5; Rare:90 | ||||
| chr2:218323276-218323441 | Rare:63; Clinvar:1 | ||||
| chr2:218398105-218398239 | Common:1; Rare:44 | ||||
| chr2:218568303-218568592 | Common:2; Rare:75 | ||||
| chr2:218659448-218659755 | Common:2; Rare:72 | ||||
| chr2:218671948-218672086 | Rare:54 | ||||
| chr2:219176899-219177041 | Common:3; Rare:41 | ||||
| chr2:219206683-219206975 | Rare:102 | ||||
| chr2:219207028-219207268 | Common:3; Rare:71 | ||||
| chr2:219229300-219229375 | Rare:21 | ||||
| chr2:219229549-219229943 | Common:2; Rare:117 | ||||
| chr2:219245383-219245534 | Common:1; Rare:44 | ||||
| chr2:219279202-219279516 | Common:2; Rare:99 |