Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6485896-6486168 | Common:1; Rare:56 | ||||
chr1:6490470-6490653 | Common:1; Rare:41 | ||||
chr1:6496545-6496656 | Rare:26 | ||||
chr1:6579744-6580075 | Common:5; Rare:111 | ||||
chr1:6602832-6603104 | Common:4; Rare:113 | ||||
chr1:7783984-7784412 | Common:6; Rare:174 | ||||
chr1:7961425-7961757 | Common:4; Rare:120; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8026201-8026466 | Common:2; Rare:122 | ||||
chr1:8423645-8423913 | Common:1; Rare:116 | ||||
chr1:8424058-8424164 | Common:1; Rare:28 | ||||
chr1:8424226-8424469 | Rare:53 | ||||
chr1:8525868-8526086 | Common:1; Rare:46 | ||||
chr1:8878578-8878838 | Rare:132 | ||||
chr1:9877891-9878052 | Rare:25 | ||||
chr1:9878055-9878115 | Common:2; Rare:11 |