| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219160766-219160935 | Common:1; Rare:50 | ||||
| chr2:219176829-219177120 | Common:8; Rare:147 | ||||
| chr2:219177818-219177933 | Common:3; Rare:24 | ||||
| chr2:219178083-219178305 | Common:13; Rare:213 | ||||
| chr2:219206670-219206968 | Rare:189 | ||||
| chr2:219207010-219207281 | Common:6; Rare:140 | ||||
| chr2:219217524-219218138 | Common:6; Rare:260; Clinvar:4 | ||||
| chr2:219229512-219229940 | Common:4; Rare:244 | ||||
| chr2:219245391-219245539 | Common:2; Rare:83 | ||||
| chr2:219279023-219279527 | Common:4; Rare:268 | ||||
| chr2:219387762-219388121 | Common:4; Rare:153 | ||||
| chr2:219388240-219388680 | Common:1; Rare:77 | ||||
| chr2:219498663-219498993 | Common:4; Rare:139 | ||||
| chr2:219543461-219544101 | Common:6; Rare:367 | ||||
| chr2:219552259-219553100 | Common:2; Rare:334; Clinvar:1; Clinvar (benign):2 |