Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:7961447-7961792 | Common:4; Rare:118; Clinvar:3; Clinvar (benign):3 | ||||
chr1:8878578-8878842 | Rare:136 | ||||
chr1:9942782-9942930 | Common:1; Rare:26 | ||||
chr1:9943025-9943100 | Rare:19 | ||||
chr1:9943251-9943509 | Common:3; Rare:74 | ||||
chr1:10032572-10032980 | Common:3; Rare:119 | ||||
chr1:10398837-10399108 | Common:2; Rare:106 | ||||
chr1:10430361-10430529 | Common:3; Rare:54 | ||||
chr1:10472435-10472640 | Rare:56 | ||||
chr1:10474821-10474984 | Rare:56; Clinvar:1 | ||||
chr1:10796617-10796815 | Common:2; Rare:61 | ||||
chr1:11099146-11099440 | Rare:66 | ||||
chr1:11099766-11099933 | Common:2; Rare:72 | ||||
chr1:11262490-11262850 | Common:2; Rare:108 | ||||
chr1:11654811-11654938 | Common:2; Rare:35 |