| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:126905290-126905473 | Rare:70 | ||||
| chr10:128047523-128047674 | Common:3; Rare:46 | ||||
| chr10:129466953-129467296 | Common:5; Rare:141; Clinvar:1 | ||||
| chr10:129701372-129701656 | Common:2; Rare:57 | ||||
| chr10:130136297-130136469 | Common:6; Rare:74 | ||||
| chr10:131981832-131982154 | Common:4; Rare:117 | ||||
| chr10:132249052-132249282 | Common:4; Rare:107 | ||||
| chr10:132331753-132332318 | Common:18; Rare:185 | ||||
| chr10:132607590-132607707 | Rare:33 | ||||
| chr10:132942467-132942672 | Common:3; Rare:54 | ||||
| chr10:133308835-133308989 | Rare:72 | ||||
| chr10:133309154-133309372 | Common:2; Rare:76 | ||||
| chr10:133357991-133358157 | Common:3; Rare:44 | ||||
| chr10:133373318-133373428 | Rare:40; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr10:133394031-133394342 | Common:2; Rare:126 |