Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21176878-21177022 | Rare:30 | ||||
chr1:21345489-21345687 | Rare:73 | ||||
chr1:21782993-21783301 | Common:2; Rare:113 | ||||
chr1:22052525-22052731 | Common:3; Rare:65 | ||||
chr1:23344229-23344576 | Common:2; Rare:115 | ||||
chr1:23368819-23368974 | Common:1; Rare:54 | ||||
chr1:23530775-23530994 | Common:1; Rare:55 | ||||
chr1:23531203-23531495 | Common:2; Rare:44 | ||||
chr1:23559407-23559656 | Common:1; Rare:107 | ||||
chr1:23627208-23627454 | Rare:61 | ||||
chr1:23691718-23691826 | Common:2; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
chr1:23691972-23692058 | Rare:25 | ||||
chr1:23743287-23743500 | Rare:81 | ||||
chr1:23778281-23778501 | Common:9; Rare:113 | ||||
chr1:23791066-23791216 | Rare:48 |