Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:166342520-166342638 | Common:2; Rare:45 | ||||
chr6:166382865-166383266 | Common:5; Rare:139 | ||||
chr6:166999081-166999405 | Common:1; Rare:111 | ||||
chr6:169701970-169702382 | Common:5; Rare:173 | ||||
chr6:169751510-169751648 | Rare:53; Clinvar (benign):2 | ||||
chr6:170553177-170553213 | Common:1; Rare:14 | ||||
chr7:727244-727298 | Rare:18; Clinvar:1 | ||||
chr7:975510-975660 | Common:1; Rare:65 | ||||
chr7:1569978-1570151 | Common:1; Rare:59 | ||||
chr7:2232886-2233033 | Rare:61 | ||||
chr7:2242171-2242275 | Common:2; Rare:58 | ||||
chr7:2354502-2354936 | Common:5; Rare:176 | ||||
chr7:4775370-4775691 | Common:7; Rare:150; Clinvar:1 | ||||
chr7:6009030-6009350 | Common:4; Rare:135; Clinvar:3; Clinvar (benign):14 | ||||
chr7:6484080-6484247 | Common:1; Rare:86 |