| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:246566149-246566584 | Common:2; Rare:149 | ||||
| chr10:988311-988466 | Rare:57 | ||||
| chr10:1048874-1049099 | Common:2; Rare:114 | ||||
| chr10:3785183-3785554 | Common:4; Rare:133 | ||||
| chr10:5813364-5813475 | Common:2; Rare:52 | ||||
| chr10:7787963-7788245 | Common:1; Rare:114 | ||||
| chr10:12195793-12196237 | Rare:118 | ||||
| chr10:13099750-13100225 | Common:4; Rare:121; Clinvar:3; Clinvar (benign):5 | ||||
| chr10:13300051-13300189 | Rare:47; Clinvar:1 | ||||
| chr10:14838046-14838352 | Common:2; Rare:80 | ||||
| chr10:14878696-14878894 | Common:1; Rare:48 | ||||
| chr10:17233582-17233929 | Common:3; Rare:111; Clinvar (benign):1 | ||||
| chr10:17643904-17644293 | Common:2; Rare:118 | ||||
| chr10:18659277-18659476 | Common:2; Rare:67 | ||||
| chr10:27100427-27100587 | Common:3; Rare:49; Clinvar:4; Clinvar (benign):2 |