Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:631708-631821 | Common:2; Rare:19 | ||||
chr1:778600-778819 | Common:4; Rare:93 | ||||
chr1:827468-827721 | Common:3; Rare:99 | ||||
chr1:2229216-2229476 | Common:1; Rare:86; Clinvar:6; Clinvar (benign):8 | ||||
chr1:3066555-3066609 | Rare:7 | ||||
chr1:3071588-3071631 | Rare:7 | ||||
chr1:3125219-3125224 | Rare:2 | ||||
chr1:3269638-3269820 | Common:12; Rare:35 | ||||
chr1:3270507-3270605 | Common:1; Rare:25 | ||||
chr1:9302807-9302967 | Common:1; Rare:35 | ||||
chr1:9342417-9342712 | Common:5; Rare:66 | ||||
chr1:9731207-9731528 | Common:4; Rare:95 | ||||
chr1:11872792-11872992 | Common:1; Rare:30 | ||||
chr1:12614933-12615273 | Common:3; Rare:49 | ||||
chr1:12619044-12619236 | Rare:39 |