| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:231241088-231241288 | Rare:107; Clinvar:3 | ||||
| chr1:231337799-231338096 | Common:4; Rare:103 | ||||
| chr1:231528616-231528733 | Common:1; Rare:49 | ||||
| chr1:234373342-234373554 | Common:1; Rare:107; Clinvar (benign):3 | ||||
| chr1:234608173-234608334 | Rare:54 | ||||
| chr1:235328127-235328356 | Common:2; Rare:71 | ||||
| chr1:243255238-243255420 | Common:1; Rare:43 | ||||
| chr1:243255741-243256128 | Common:1; Rare:107; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:246566141-246566594 | Common:3; Rare:152 | ||||
| chr1:246724268-246724428 | Common:2; Rare:62 | ||||
| chr10:988325-988479 | Common:1; Rare:66 | ||||
| chr10:1048880-1049095 | Common:2; Rare:110 | ||||
| chr10:1056731-1056823 | Common:2; Rare:39 | ||||
| chr10:3785180-3785554 | Common:4; Rare:135 | ||||
| chr10:5813413-5813612 | Common:2; Rare:81 |