| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:110407616-110407798 | Common:2; Rare:84 | ||||
| chr1:111140046-111140269 | Common:1; Rare:80 | ||||
| chr1:111739367-111739551 | Common:1; Rare:45 | ||||
| chr1:112395981-112396258 | Common:1; Rare:87 | ||||
| chr1:112619099-112619205 | Rare:37 | ||||
| chr1:112619675-112619871 | Common:1; Rare:74 | ||||
| chr1:112674501-112674743 | Common:1; Rare:41 | ||||
| chr1:112956159-112956473 | Common:5; Rare:135; Clinvar:9; Clinvar (benign):3 | ||||
| chr1:113905006-113905442 | Common:5; Rare:125 | ||||
| chr1:114716713-114716874 | Common:1; Rare:73; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:114780569-114780750 | Rare:68 | ||||
| chr1:115089455-115089591 | Common:2; Rare:53 | ||||
| chr1:117060072-117060360 | Common:6; Rare:73 | ||||
| chr1:117929560-117929792 | Common:1; Rare:69 | ||||
| chr1:119140573-119140748 | Rare:64; Clinvar (pathogenic):1 |