| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:123008769-123009026 | Common:6; Rare:68; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124418888-124419092 | Common:4; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:124461706-124461856 | Common:5; Rare:53 | ||||
| chr10:124791810-124792003 | Common:2; Rare:98 | ||||
| chr10:124801645-124801832 | Rare:57 | ||||
| chr10:125719453-125719770 | Common:1; Rare:116 | ||||
| chr10:125823192-125823628 | Common:1; Rare:155; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:125896272-125896624 | Common:5; Rare:31 | ||||
| chr10:126905255-126905473 | Rare:86 | ||||
| chr10:132331792-132332155 | Common:16; Rare:120 | ||||
| chr10:133308835-133308990 | Rare:72 | ||||
| chr11:207352-207726 | Common:8; Rare:126 | ||||
| chr11:208688-208857 | Rare:69 | ||||
| chr11:236333-236523 | Common:6; Rare:57 | ||||
| chr11:236913-237044 | Common:1; Rare:51 |