Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94820147-94820416 | Common:4; Rare:70 | ||||
chr1:95072829-95073032 | Common:2; Rare:80; Clinvar (benign):2 | ||||
chr1:95233908-95234243 | Common:5; Rare:103 | ||||
chr1:96721600-96721844 | Common:2; Rare:113 | ||||
chr1:98661575-98661881 | Common:2; Rare:105 | ||||
chr1:99766620-99766695 | Rare:14 | ||||
chr1:99850016-99850143 | Rare:48 | ||||
chr1:99969891-99970069 | Rare:45 | ||||
chr1:100037973-100038187 | Common:1; Rare:84 | ||||
chr1:100132887-100133233 | Common:2; Rare:134 | ||||
chr1:100178167-100178352 | Common:2; Rare:25 | ||||
chr1:100266107-100266420 | Common:4; Rare:111 | ||||
chr1:100894639-100894917 | Common:2; Rare:67 | ||||
chr1:100895139-100895202 | Rare:9 | ||||
chr1:100895927-100896149 | Rare:62 |