Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114581571-114581879 | Common:1; Rare:131 | ||||
chr1:114669988-114670269 | Common:1; Rare:89 | ||||
chr1:114670429-114670579 | Rare:52 | ||||
chr1:114716674-114716885 | Common:1; Rare:90; Clinvar:5; Clinvar (benign):2 | ||||
chr1:114757428-114757607 | Rare:41 | ||||
chr1:114757931-114758190 | Common:3; Rare:81 | ||||
chr1:114780404-114780807 | Common:1; Rare:143 | ||||
chr1:115641776-115641940 | Rare:61 | ||||
chr1:115642846-115642970 | Common:1; Rare:28 | ||||
chr1:115671543-115671695 | Common:1; Rare:33 | ||||
chr1:115976400-115976690 | Rare:107 | ||||
chr1:116373041-116373304 | Rare:83 | ||||
chr1:116570345-116570593 | Rare:54 | ||||
chr1:116570970-116571172 | Common:2; Rare:60 | ||||
chr1:116667659-116667927 | Common:2; Rare:94 |