Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112956188-112956417 | Common:4; Rare:105; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113979307-113979502 | Rare:50 | ||||
chr1:117929605-117929792 | Rare:49 | ||||
chr1:119140637-119140767 | Rare:40 | ||||
chr1:145823937-145824238 | Rare:106 | ||||
chr1:145927433-145927644 | Common:1; Rare:59; Clinvar (pathogenic):1 | ||||
chr1:145964484-145964748 | Rare:61 | ||||
chr1:149886646-149886942 | Common:1; Rare:97 | ||||
chr1:149887953-149888215 | Rare:55 | ||||
chr1:149927760-149927922 | Common:1; Rare:65; Clinvar (benign):4 | ||||
chr1:151165889-151166157 | Common:3; Rare:77 | ||||
chr1:151763459-151763584 | Common:1; Rare:47 | ||||
chr1:151993766-151994037 | Common:4; Rare:101 | ||||
chr1:153545803-153545916 | Rare:21 | ||||
chr1:153608941-153609153 | Rare:42 |