| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:111140021-111140305 | Common:3; Rare:95 | ||||
| chr1:111447553-111447826 | Common:1; Rare:54 | ||||
| chr1:111619606-111619948 | Common:2; Rare:107 | ||||
| chr1:111619964-111620142 | Common:1; Rare:50 | ||||
| chr1:111739268-111739560 | Common:3; Rare:92 | ||||
| chr1:111755533-111755845 | Common:4; Rare:105 | ||||
| chr1:112619658-112619879 | Common:2; Rare:81 | ||||
| chr1:112674619-112675014 | Common:2; Rare:94 | ||||
| chr1:112703843-112703917 | Common:1; Rare:11 | ||||
| chr1:112707068-112707219 | Rare:50 | ||||
| chr1:112956036-112956307 | Common:4; Rare:88; Clinvar:9; Clinvar (benign):3 | ||||
| chr1:112956316-112956868 | Common:5; Rare:139; Clinvar:2 | ||||
| chr1:113073085-113073247 | Common:1; Rare:59 | ||||
| chr1:113759458-113759598 | Common:2; Rare:43 | ||||
| chr1:113904721-113905385 | Common:7; Rare:200; Clinvar (benign):2 |