| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:108692091-108692803 | Common:20; Rare:867 | ||||
| chr1:108692764-108693577 | Rare:335 | ||||
| chr1:108746385-108746785 | Common:11; Rare:580 | ||||
| chr1:108747156-108747556 | Common:1; Rare:81 | ||||
| chr1:108781237-108782093 | Common:9; Rare:184 | ||||
| chr1:108830449-108830933 | Common:11; Rare:329 | ||||
| chr1:108876752-108877215 | Common:8; Rare:375; Clinvar:23; Clinvar (benign):4 | ||||
| chr1:108963075-108963712 | Common:14; Rare:673 | ||||
| chr1:109040800-109041673 | Common:9; Rare:283 | ||||
| chr1:109041630-109042030 | Rare:140 | ||||
| chr1:109041997-109042476 | Common:19; Rare:409 | ||||
| chr1:109075829-109076229 | Common:2; Rare:589 | ||||
| chr1:109089114-109089555 | Common:5; Rare:172 | ||||
| chr1:109090025-109090425 | Common:7; Rare:118 | ||||
| chr1:109090440-109091505 | Common:34; Rare:947 |