| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:111739361-111739561 | Common:3; Rare:51 | ||||
| chr1:112395990-112396262 | Common:1; Rare:84 | ||||
| chr1:112619109-112619236 | Rare:45 | ||||
| chr1:112619634-112619883 | Common:2; Rare:88 | ||||
| chr1:112703735-112703933 | Common:1; Rare:49 | ||||
| chr1:112956117-112956461 | Common:5; Rare:138; Clinvar:10; Clinvar (benign):3 | ||||
| chr1:113073052-113073238 | Common:1; Rare:70 | ||||
| chr1:113390176-113390488 | Common:1; Rare:78 | ||||
| chr1:113812217-113812612 | Common:2; Rare:158 | ||||
| chr1:113905018-113905429 | Common:5; Rare:116 | ||||
| chr1:113930631-113930724 | Common:1; Rare:22 | ||||
| chr1:113930737-113931023 | Rare:56 | ||||
| chr1:114581539-114581832 | Common:1; Rare:131 | ||||
| chr1:114669993-114670259 | Common:1; Rare:85 | ||||
| chr1:114716146-114716453 | Common:2; Rare:70; Clinvar (benign):1 |