Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19485436-19485893 | Common:1; Rare:167 | ||||
chr1:19485926-19486102 | Common:1; Rare:61 | ||||
chr1:19596577-19597205 | Common:5; Rare:196 | ||||
chr1:19597414-19597550 | Common:2; Rare:36 | ||||
chr1:19799265-19799464 | Common:3; Rare:41 | ||||
chr1:19799646-19799907 | Common:4; Rare:65 | ||||
chr1:19800167-19800525 | Common:3; Rare:77 | ||||
chr1:19882173-19882480 | Common:3; Rare:91 | ||||
chr1:19882891-19882981 | Common:1; Rare:19 | ||||
chr1:20507847-20507908 | Rare:21 | ||||
chr1:20507986-20508272 | Common:3; Rare:92 | ||||
chr1:20661286-20661798 | Common:3; Rare:176; Clinvar:4; Clinvar (benign):7 | ||||
chr1:20785894-20786050 | Rare:31 | ||||
chr1:20786493-20786978 | Rare:178 | ||||
chr1:20787234-20787685 | Common:1; Rare:195 |