| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:179081889-179082114 | Common:1; Rare:70 | ||||
| chr1:179082449-179082613 | Common:1; Rare:35 | ||||
| chr1:179143042-179143245 | Rare:39 | ||||
| chr1:179228906-179229133 | Rare:50 | ||||
| chr1:179229495-179229810 | Common:7; Rare:85 | ||||
| chr1:179293677-179293884 | Common:3; Rare:66 | ||||
| chr1:179294030-179294210 | Common:1; Rare:41 | ||||
| chr1:179365637-179365783 | Common:5; Rare:43 | ||||
| chr1:179365819-179366131 | Common:11; Rare:66 | ||||
| chr1:179366228-179366235 | Common:1; Rare:1 | ||||
| chr1:179877715-179877905 | Rare:41 | ||||
| chr1:179881919-179881941 | Rare:4 | ||||
| chr1:179881979-179882358 | Common:4; Rare:89 | ||||
| chr1:179882367-179883026 | Common:3; Rare:292; Clinvar:11; Clinvar (benign):5 | ||||
| chr1:179883294-179883373 | Common:1; Rare:19 |