Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:45111669-45111822 | Common:1; Rare:58 | ||||
chr7:47979500-47979770 | Common:1; Rare:103 | ||||
chr7:50450305-50450453 | Common:1; Rare:59 | ||||
chr7:50561034-50561207 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
chr7:50782894-50783157 | Rare:69 | ||||
chr7:54542089-54542521 | Common:3; Rare:113 | ||||
chr7:54542537-54542644 | Common:1; Rare:16 | ||||
chr7:55365073-55365351 | Common:2; Rare:74 | ||||
chr7:55365455-55365746 | Common:3; Rare:87 | ||||
chr7:55365885-55366073 | Rare:74 | ||||
chr7:55366234-55366408 | Common:1; Rare:80 | ||||
chr7:55572283-55572694 | Common:2; Rare:139 | ||||
chr7:55887381-55887502 | Common:1; Rare:35 | ||||
chr7:55887595-55887671 | Common:3; Rare:26 | ||||
chr7:55951773-55951953 | Rare:51 |