| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:238426886-238427067 | Common:1; Rare:66 | ||||
| chr2:240025276-240025488 | Common:3; Rare:83; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240136252-240136382 | Rare:50 | ||||
| chr2:240819274-240819562 | Common:2; Rare:68 | ||||
| chr2:240820194-240820440 | Rare:50 | ||||
| chr2:241102259-241102393 | Common:2; Rare:50 | ||||
| chr2:241149434-241149615 | Common:3; Rare:59 | ||||
| chr2:241239812-241239833 | Rare:5 | ||||
| chr2:241242577-241242769 | Rare:49 | ||||
| chr2:241272794-241272976 | Rare:71 | ||||
| chr2:241315128-241315398 | Common:5; Rare:88 | ||||
| chr2:241315633-241315987 | Common:5; Rare:137 | ||||
| chr2:241508503-241508833 | Common:2; Rare:102 | ||||
| chr2:241509337-241509527 | Rare:43 | ||||
| chr2:241637544-241637709 | Common:1; Rare:90 |