| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:88990444-88990643 | Common:3; Rare:52; Clinvar (benign):3 | ||||
| chr10:89327942-89328015 | Common:1; Rare:10 | ||||
| chr10:89332415-89332529 | Common:3; Rare:19 | ||||
| chr10:89414671-89414778 | Common:2; Rare:50 | ||||
| chr10:89701409-89701638 | Common:1; Rare:66 | ||||
| chr10:91633039-91633337 | Common:2; Rare:93 | ||||
| chr10:92574013-92574137 | Common:1; Rare:37 | ||||
| chr10:93482213-93482334 | Common:2; Rare:39 | ||||
| chr10:93702501-93702714 | Common:4; Rare:75 | ||||
| chr10:93757735-93758039 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:95693906-95693979 | Common:1; Rare:28; Clinvar (benign):1 | ||||
| chr10:95907865-95907939 | Common:1; Rare:23 | ||||
| chr10:96129969-96130067 | Common:1; Rare:32 | ||||
| chr10:96130219-96130540 | Common:1; Rare:109 | ||||
| chr10:97426037-97426298 | Common:2; Rare:113 |