Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10398734-10399125 | Common:2; Rare:144 | ||||
chr1:10399293-10399705 | Common:3; Rare:120 | ||||
chr1:10415530-10415665 | Rare:17 | ||||
chr1:10430345-10430814 | Common:8; Rare:155 | ||||
chr1:10472444-10472657 | Rare:56 | ||||
chr1:11099357-11099453 | Rare:22 | ||||
chr1:11099740-11099939 | Common:3; Rare:80 | ||||
chr1:11262490-11262851 | Common:2; Rare:109 | ||||
chr1:11273437-11273515 | Common:1; Rare:28; Clinvar (benign):1 | ||||
chr1:11654838-11654925 | Common:1; Rare:19 | ||||
chr1:11736006-11736187 | Common:3; Rare:56 | ||||
chr1:11805935-11806257 | Common:2; Rare:87; Clinvar:1 | ||||
chr1:11934576-11934758 | Common:2; Rare:64; Clinvar:5; Clinvar (benign):1 | ||||
chr1:11979948-11980374 | Common:4; Rare:109; Clinvar:1; Clinvar (benign):2 | ||||
chr1:12596049-12596136 | Rare:16 |