| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:122953800-122954110 | Common:1; Rare:84 | ||||
| chr10:122954130-122954660 | Common:7; Rare:916 | ||||
| chr10:122980177-122980911 | Common:16; Rare:452 | ||||
| chr10:123008165-123008565 | Common:4; Rare:110 | ||||
| chr10:123008671-123009096 | Common:42; Rare:597; Clinvar:29; Clinvar (benign):37 | ||||
| chr10:123009439-123009839 | Common:4; Rare:73 | ||||
| chr10:123135094-123135785 | Common:6; Rare:557 | ||||
| chr10:123135710-123136687 | Common:10; Rare:705 | ||||
| chr10:123147751-123148254 | Common:7; Rare:381 | ||||
| chr10:123153970-123154499 | Common:32; Rare:668 | ||||
| chr10:123154557-123155328 | Common:4; Rare:492 | ||||
| chr10:123162220-123162710 | Rare:111 | ||||
| chr10:124417953-124418427 | Common:4; Rare:133 | ||||
| chr10:124418337-124418737 | Common:9; Rare:160 | ||||
| chr10:124418805-124419205 | Common:35; Rare:793; Clinvar:20; Clinvar (benign):7 |