Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11654421-11654477 | Rare:17 | ||||
chr1:11654800-11654918 | Common:2; Rare:32 | ||||
chr1:11663949-11664273 | Common:2; Rare:82 | ||||
chr1:11691514-11691710 | Common:3; Rare:41 | ||||
chr1:11735765-11736196 | Common:3; Rare:107 | ||||
chr1:11805888-11806286 | Common:2; Rare:114; Clinvar:1 | ||||
chr1:11807047-11807191 | Common:1; Rare:42 | ||||
chr1:11926268-11926596 | Common:6; Rare:88 | ||||
chr1:11934480-11934779 | Common:5; Rare:96; Clinvar:5; Clinvar (benign):1 | ||||
chr1:11934789-11934853 | Rare:12; Clinvar:1 | ||||
chr1:11980081-11980479 | Common:6; Rare:127; Clinvar:1; Clinvar (benign):5 | ||||
chr1:12019284-12019556 | Common:5; Rare:99 | ||||
chr1:12596111-12596349 | Common:4; Rare:45 | ||||
chr1:12616619-12616842 | Common:1; Rare:43 | ||||
chr1:12617203-12617804 | Common:2; Rare:117 |