| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:125823200-125823568 | Common:1; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:125896282-125896628 | Common:5; Rare:29 | ||||
| chr10:128047442-128047635 | Common:2; Rare:63 | ||||
| chr10:129466987-129467282 | Common:4; Rare:112; Clinvar:1 | ||||
| chr10:132331792-132332164 | Common:16; Rare:123 | ||||
| chr10:133308829-133308989 | Rare:75 | ||||
| chr11:207343-207720 | Common:8; Rare:129 | ||||
| chr11:208662-208857 | Rare:76 | ||||
| chr11:236326-236525 | Common:6; Rare:64 | ||||
| chr11:236896-237044 | Common:1; Rare:56 | ||||
| chr11:313883-314099 | Rare:40 | ||||
| chr11:394062-394216 | Common:1; Rare:38 | ||||
| chr11:441959-442063 | Rare:38 | ||||
| chr11:506728-507007 | Common:3; Rare:94 | ||||
| chr11:560729-561021 | Common:5; Rare:132 |