| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:114510800-114511365 | Common:10; Rare:400 | ||||
| chr1:114581601-114581851 | Rare:101 | ||||
| chr1:114669980-114670310 | Common:2; Rare:180 | ||||
| chr1:114716697-114716881 | Common:1; Rare:124; Clinvar:6; Clinvar (benign):1 | ||||
| chr1:114756970-114757870 | Common:4; Rare:300 | ||||
| chr1:114757895-114758112 | Common:6; Rare:128 | ||||
| chr1:114780459-114780809 | Common:2; Rare:222 | ||||
| chr1:115641613-115642039 | Common:5; Rare:123; Clinvar:1; Clinvar (benign):2 | ||||
| chr1:115975820-115976670 | Common:2; Rare:350 | ||||
| chr1:115976690-115977070 | Common:3; Rare:135 | ||||
| chr1:116373171-116374148 | Common:4; Rare:370 | ||||
| chr1:116570898-116571168 | Common:6; Rare:134 | ||||
| chr1:116667657-116667890 | Common:2; Rare:143 | ||||
| chr1:116909858-116910020 | Rare:39 | ||||
| chr1:117059988-117060382 | Common:14; Rare:205 |