Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:17439662-17439901 | Rare:80 | ||||
chr1:18902535-18902859 | Rare:97; Clinvar:7 | ||||
chr1:19210071-19210533 | Common:1; Rare:150 | ||||
chr1:19251494-19251876 | Common:6; Rare:129 | ||||
chr1:19311996-19312358 | Common:8; Rare:169 | ||||
chr1:19485439-19485762 | Common:1; Rare:120 | ||||
chr1:19596846-19597105 | Common:2; Rare:113 | ||||
chr1:19799707-19799987 | Common:5; Rare:87 | ||||
chr1:20486201-20486398 | Rare:46 | ||||
chr1:20508063-20508240 | Common:2; Rare:63 | ||||
chr1:20661206-20661245 | Rare:13 | ||||
chr1:20661265-20661310 | Common:1; Rare:15; Clinvar:1; Clinvar (benign):1 | ||||
chr1:20661331-20661736 | Common:3; Rare:148; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786573-20786859 | Rare:106 | ||||
chr1:20787206-20787465 | Rare:121 |