Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1013382-1013514 | Common:3; Rare:41 | ||||
chr1:1324604-1324900 | Common:3; Rare:148 | ||||
chr1:1399296-1399575 | Common:1; Rare:120 | ||||
chr1:1658935-1659060 | Common:1; Rare:47 | ||||
chr1:1724289-1724440 | Common:3; Rare:50 | ||||
chr1:2391540-2391888 | Common:2; Rare:129 | ||||
chr1:3857209-3857473 | Common:1; Rare:70 | ||||
chr1:3900219-3900352 | Common:10; Rare:66 | ||||
chr1:6199514-6199809 | Common:2; Rare:107 | ||||
chr1:6208680-6208851 | Common:1; Rare:45 | ||||
chr1:6701780-6701997 | Rare:67 | ||||
chr1:7771177-7771352 | Common:3; Rare:78 | ||||
chr1:7961455-7961757 | Common:4; Rare:105; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8878578-8878835 | Rare:130 | ||||
chr1:9943280-9943488 | Common:2; Rare:53 |