Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16644645-16644826 | Common:1; Rare:3 | ||||
chr1:16645493-16645603 | Common:2; Rare:2 | ||||
chr1:16889372-16889596 | Common:5; Rare:47 | ||||
chr1:16895604-16895980 | Common:6; Rare:75 | ||||
chr1:16904828-16904984 | Common:1; Rare:18 | ||||
chr1:16913883-16914121 | Common:8; Rare:49 | ||||
chr1:19242343-19242576 | Common:1; Rare:73; Clinvar:1 | ||||
chr1:20554504-20554647 | Rare:26 | ||||
chr1:21759603-21759726 | Common:2; Rare:23 | ||||
chr1:21884836-21885151 | Common:1; Rare:93; Clinvar:1; Clinvar (benign):1 | ||||
chr1:22025188-22025552 | Common:8; Rare:97 | ||||
chr1:22456427-22456612 | Rare:33 | ||||
chr1:24321871-24321997 | Common:1; Rare:32 | ||||
chr1:25829145-25829377 | Common:5; Rare:41 | ||||
chr1:25875487-25875666 | Rare:53 |