Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19240386-19240539 | Common:1; Rare:42 | ||||
chr1:19251422-19251879 | Common:6; Rare:156 | ||||
chr1:19312046-19312356 | Common:8; Rare:149 | ||||
chr1:19484310-19484568 | Common:1; Rare:90 | ||||
chr1:19485431-19485726 | Common:1; Rare:94 | ||||
chr1:19485974-19486010 | Common:1; Rare:9 | ||||
chr1:19596882-19597119 | Common:2; Rare:112 | ||||
chr1:20485645-20485946 | Common:1; Rare:51 | ||||
chr1:20486196-20486376 | Rare:40 | ||||
chr1:20507991-20508261 | Common:3; Rare:88 | ||||
chr1:20661171-20661730 | Common:4; Rare:199; Clinvar:5; Clinvar (benign):9 | ||||
chr1:20685261-20685385 | Common:1; Rare:26 | ||||
chr1:20786591-20786916 | Rare:125 | ||||
chr1:20787196-20787450 | Rare:119 | ||||
chr1:20787509-20787561 | Rare:17 |