| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:101236611-101237040 | Common:5; Rare:84 | ||||
| chr1:108200154-108200451 | Common:9; Rare:91 | ||||
| chr1:108692189-108692357 | Common:1; Rare:63 | ||||
| chr1:109090665-109090841 | Common:3; Rare:37 | ||||
| chr1:109656274-109656357 | Rare:21 | ||||
| chr1:110339154-110339443 | Common:1; Rare:81 | ||||
| chr1:110407616-110407820 | Common:3; Rare:93 | ||||
| chr1:111140050-111140266 | Common:1; Rare:75 | ||||
| chr1:112619105-112619199 | Rare:33 | ||||
| chr1:112619773-112619851 | Common:1; Rare:30 | ||||
| chr1:112956061-112956433 | Common:4; Rare:138; Clinvar:12; Clinvar (benign):3 | ||||
| chr1:113073081-113073241 | Common:1; Rare:56 | ||||
| chr1:113905026-113905366 | Common:3; Rare:93 | ||||
| chr1:114581601-114581841 | Rare:96 | ||||
| chr1:114716713-114717046 | Common:4; Rare:121; Clinvar:5; Clinvar (benign):1 |