| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218322976-218323386 | Common:6; Rare:142 | ||||
| chr2:218381904-218382258 | Common:2; Rare:72 | ||||
| chr2:218514426-218514536 | Common:2; Rare:11 | ||||
| chr2:218568046-218568087 | Rare:9 | ||||
| chr2:218568088-218568117 | Rare:7 | ||||
| chr2:218568192-218568688 | Common:6; Rare:123 | ||||
| chr2:218568733-218568978 | Common:1; Rare:68 | ||||
| chr2:218569284-218569322 | Rare:5 | ||||
| chr2:218609656-218609780 | Rare:21 | ||||
| chr2:218659334-218659793 | Common:4; Rare:117 | ||||
| chr2:218671958-218672382 | Common:2; Rare:113 | ||||
| chr2:218710701-218711005 | Common:3; Rare:72 | ||||
| chr2:218745927-218746163 | Common:1; Rare:46 | ||||
| chr2:218782029-218782297 | Rare:84; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:218959445-218959534 | Rare:26 |