Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94418169-94418481 | Common:2; Rare:115 | ||||
chr1:94541730-94541991 | Rare:76 | ||||
chr1:94926839-94927497 | Common:4; Rare:209 | ||||
chr1:95233945-95234260 | Common:5; Rare:99 | ||||
chr1:98661616-98661875 | Common:2; Rare:93 | ||||
chr1:99646178-99646358 | Rare:42 | ||||
chr1:99850017-99850663 | Rare:163; Clinvar:3; Clinvar (benign):2 | ||||
chr1:99969922-99970069 | Rare:43 | ||||
chr1:100037996-100038178 | Common:1; Rare:72 | ||||
chr1:100132908-100133202 | Common:2; Rare:105 | ||||
chr1:100266097-100266301 | Common:3; Rare:75 | ||||
chr1:100894778-100894914 | Common:1; Rare:29 | ||||
chr1:100895958-100896149 | Rare:52 | ||||
chr1:101025763-101025910 | Common:1; Rare:44 | ||||
chr1:101026103-101026316 | Rare:36 |