Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:9823915-9824226 | Common:1; Rare:98 | ||||
chr1:9824434-9824834 | Common:1; Rare:124 | ||||
chr1:9910178-9910730 | Common:5; Rare:179 | ||||
chr1:9943244-9943516 | Common:3; Rare:78 | ||||
chr1:10032540-10033030 | Common:4; Rare:135 | ||||
chr1:10033131-10033278 | Rare:31 | ||||
chr1:10033420-10033820 | Common:2; Rare:128 | ||||
chr1:10171060-10171390 | Rare:61 | ||||
chr1:10179025-10179415 | Common:3; Rare:76 | ||||
chr1:10210265-10210615 | Common:6; Rare:103 | ||||
chr1:10398865-10399121 | Common:2; Rare:100 | ||||
chr1:10430625-10430804 | Common:5; Rare:63 | ||||
chr1:10472453-10472659 | Rare:52 | ||||
chr1:10474861-10475218 | Common:1; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
chr1:10651469-10651622 | Common:1; Rare:32 |