| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:111739339-111739579 | Common:3; Rare:65 | ||||
| chr1:112396062-112396257 | Common:1; Rare:62 | ||||
| chr1:112619091-112619236 | Rare:54 | ||||
| chr1:112619682-112619875 | Common:2; Rare:72 | ||||
| chr1:112956150-112956467 | Common:5; Rare:135; Clinvar:10; Clinvar (benign):3 | ||||
| chr1:113073081-113073223 | Common:1; Rare:47 | ||||
| chr1:113390209-113390471 | Common:1; Rare:68 | ||||
| chr1:113812273-113812593 | Common:2; Rare:124 | ||||
| chr1:113905022-113905365 | Common:3; Rare:94 | ||||
| chr1:114581588-114581912 | Rare:127 | ||||
| chr1:114716671-114716862 | Common:1; Rare:78; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:114757931-114758108 | Common:3; Rare:59 | ||||
| chr1:116570970-116571168 | Common:2; Rare:60 | ||||
| chr1:117929546-117929800 | Common:2; Rare:75 | ||||
| chr1:119140584-119140744 | Rare:58; Clinvar (pathogenic):1 |