Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11847977-11848182 | Common:2; Rare:44 | ||||
chr1:11848344-11848555 | Common:2; Rare:45 | ||||
chr1:11858688-11859152 | Common:2; Rare:146 | ||||
chr1:11979904-11980512 | Common:6; Rare:164; Clinvar:1; Clinvar (benign):7 | ||||
chr1:11981846-11982007 | Common:12; Rare:26; Clinvar (benign):2 | ||||
chr1:12617673-12617883 | Common:5; Rare:19 | ||||
chr1:12618189-12618439 | Common:1; Rare:54 | ||||
chr1:15409784-15409910 | Rare:40 | ||||
chr1:15526550-15526917 | Common:2; Rare:119 | ||||
chr1:16017756-16018266 | Common:9; Rare:183 | ||||
chr1:16352400-16352587 | Common:3; Rare:102 | ||||
chr1:19210234-19210417 | Rare:70 | ||||
chr1:19251505-19251838 | Common:6; Rare:109 | ||||
chr1:19312142-19312343 | Common:5; Rare:89 | ||||
chr1:19596453-19596545 | Rare:21 |