Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89994973-89995184 | Common:2; Rare:76 | ||||
chr1:91021936-91022214 | Rare:80 | ||||
chr1:91022226-91022360 | Rare:20 | ||||
chr1:91500736-91500925 | Common:2; Rare:61 | ||||
chr1:91501074-91501153 | Rare:20 | ||||
chr1:91501295-91501545 | Rare:58 | ||||
chr1:92298908-92299089 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
chr1:92785054-92785265 | Common:3; Rare:82 | ||||
chr1:92831874-92832120 | Common:1; Rare:108; Clinvar:7; Clinvar (benign):5 | ||||
chr1:93079064-93079303 | Common:3; Rare:103 | ||||
chr1:93179902-93180006 | Rare:28 | ||||
chr1:93180053-93180108 | Rare:20 | ||||
chr1:93180110-93180216 | Rare:39 | ||||
chr1:93180220-93180762 | Common:2; Rare:214 | ||||
chr1:93345641-93345979 | Common:5; Rare:117 |