Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:8817164-8817310 | Rare:41 | ||||
chr1:8878578-8878842 | Rare:136 | ||||
chr1:9910340-9910669 | Common:3; Rare:106 | ||||
chr1:9943219-9943505 | Common:3; Rare:78 | ||||
chr1:9997067-9997284 | Common:2; Rare:65 | ||||
chr1:10032756-10033095 | Common:2; Rare:88 | ||||
chr1:10398857-10399108 | Common:2; Rare:96 | ||||
chr1:10399302-10399508 | Common:3; Rare:45 | ||||
chr1:10474870-10475028 | Rare:61; Clinvar:4; Clinvar (benign):1 | ||||
chr1:11012557-11012690 | Common:1; Rare:42; Clinvar:3; Clinvar (benign):1 | ||||
chr1:11099784-11099899 | Rare:56 | ||||
chr1:11189275-11189380 | Rare:19 | ||||
chr1:11262484-11262828 | Common:2; Rare:107 | ||||
chr1:11273430-11273510 | Common:1; Rare:26; Clinvar (benign):1 | ||||
chr1:11654417-11654487 | Rare:21 |