Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:183023052-183023286 | Common:5; Rare:60 | ||||
chr1:183023772-183024141 | Common:1; Rare:118 | ||||
chr1:183185960-183185963 | |||||
chr1:183186045-183186355 | Common:6; Rare:79; Clinvar:5; Clinvar (benign):5 | ||||
chr1:183472261-183472576 | Common:2; Rare:106 | ||||
chr1:183590411-183590681 | Common:3; Rare:52; Clinvar (benign):2 | ||||
chr1:183590891-183591064 | Common:3; Rare:33 | ||||
chr1:183635570-183636110 | Common:5; Rare:147 | ||||
chr1:183805017-183805243 | Rare:60 | ||||
chr1:184051666-184051796 | Common:2; Rare:55 | ||||
chr1:184386732-184387187 | Common:4; Rare:127 | ||||
chr1:184387224-184387368 | Rare:25 | ||||
chr1:184754579-184754724 | Common:2; Rare:62 | ||||
chr1:184754800-184755075 | Common:1; Rare:64 | ||||
chr1:184974396-184974661 | Rare:68 |