Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:3625674-3625749 | Common:1; Rare:35 | ||||
chr1:8359869-8360166 | Rare:99; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:8422528-8422763 | Rare:59 | ||||
chr1:9182107-9182193 | Rare:22 | ||||
chr1:9182282-9182350 | Rare:19 | ||||
chr1:9182354-9182471 | Common:2; Rare:36 | ||||
chr1:9731261-9731654 | Common:5; Rare:109 | ||||
chr1:10785184-10785449 | Common:1; Rare:43 | ||||
chr1:12231042-12231239 | Common:2; Rare:43 | ||||
chr1:12618584-12618692 | Common:1; Rare:24 | ||||
chr1:12619105-12619236 | Rare:28 | ||||
chr1:15426849-15427257 | Common:1; Rare:120 | ||||
chr1:15573667-15573784 | Common:1; Rare:35 | ||||
chr1:15760164-15760449 | Rare:54 | ||||
chr1:15800227-15800582 | Common:2; Rare:68 |