Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:127588268-127588501 | Rare:98 | ||||
chr7:127651848-127652227 | Common:2; Rare:110 | ||||
chr7:128409908-128410072 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
chr7:128455663-128455931 | Common:3; Rare:135 | ||||
chr7:128476633-128476760 | Common:2; Rare:42 | ||||
chr7:128739152-128739427 | Common:2; Rare:73 | ||||
chr7:129054885-129055226 | Common:2; Rare:65 | ||||
chr7:129611623-129611748 | Common:1; Rare:35 | ||||
chr7:130205380-130205496 | Rare:55 | ||||
chr7:131327711-131327902 | Rare:65 | ||||
chr7:134316867-134317175 | Common:2; Rare:88 | ||||
chr7:134646566-134646864 | Common:6; Rare:89 | ||||
chr7:134986362-134986556 | Common:4; Rare:71 | ||||
chr7:135148002-135148144 | Rare:37 | ||||
chr7:135662440-135662562 | Common:2; Rare:63 |