Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39738736-39738910 | Common:2; Rare:37 | ||||
chr1:39883454-39883575 | Common:1; Rare:51; Clinvar (pathogenic):1 | ||||
chr1:39954963-39955222 | Common:1; Rare:68 | ||||
chr1:40040425-40040814 | Common:3; Rare:123 | ||||
chr1:40097207-40097282 | Rare:35; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
chr1:40161276-40161402 | Rare:32 | ||||
chr1:40257898-40258274 | Common:4; Rare:104; Clinvar:8 | ||||
chr1:40449992-40450145 | Common:1; Rare:63 | ||||
chr1:40508626-40508816 | Common:6; Rare:57 | ||||
chr1:40531487-40531731 | Common:1; Rare:68 | ||||
chr1:40691504-40691832 | Common:2; Rare:156 | ||||
chr1:40692014-40692286 | Common:2; Rare:88 | ||||
chr1:40979610-40979806 | Common:2; Rare:65 | ||||
chr1:41242110-41242327 | Rare:66 | ||||
chr1:42335169-42335366 | Common:5; Rare:98 |