Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:86396020-86396101 | Common:1; Rare:24 | ||||
chr1:86396251-86396413 | Common:3; Rare:39 | ||||
chr1:86704416-86704868 | Common:2; Rare:175 | ||||
chr1:86914392-86914755 | Rare:109 | ||||
chr1:88684070-88684350 | Common:3; Rare:76 | ||||
chr1:88891485-88891741 | Common:1; Rare:107 | ||||
chr1:88992641-88992978 | Common:1; Rare:83 | ||||
chr1:89994955-89995170 | Common:2; Rare:82 | ||||
chr1:91021963-91022197 | Rare:71 | ||||
chr1:91500740-91500890 | Common:2; Rare:49 | ||||
chr1:92029901-92030002 | Rare:31 | ||||
chr1:92298945-92299076 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
chr1:93079018-93079303 | Common:3; Rare:122 | ||||
chr1:93180285-93180738 | Common:1; Rare:180 | ||||
chr1:93345772-93345979 | Common:4; Rare:84 |