| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:133307800-133308007 | Common:2; Rare:51 | ||||
| chr10:133308480-133308569 | Rare:28 | ||||
| chr10:133308780-133309019 | Common:1; Rare:107 | ||||
| chr10:133309068-133309441 | Common:2; Rare:145 | ||||
| chr10:133357313-133357548 | Common:2; Rare:42 | ||||
| chr10:133357628-133357880 | Common:2; Rare:42 | ||||
| chr10:133357918-133358041 | Common:2; Rare:39 | ||||
| chr10:133373278-133373582 | Common:2; Rare:132; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr10:133373683-133373772 | Common:1; Rare:36 | ||||
| chr10:133378530-133378798 | Common:3; Rare:45 | ||||
| chr10:133378839-133379332 | Common:21; Rare:106 | ||||
| chr10:133393958-133394566 | Common:3; Rare:235 | ||||
| chr10:133394573-133394632 | Rare:16 | ||||
| chr10:133520134-133520482 | Common:4; Rare:95 | ||||
| chr11:207289-207816 | Common:9; Rare:165 |