Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882478-179882898 | Rare:208; Clinvar:9; Clinvar (benign):2 | ||||
chr1:179954694-179954822 | Rare:29 | ||||
chr1:180631861-180632169 | Common:5; Rare:112 | ||||
chr1:181022827-181023241 | Common:25; Rare:188 | ||||
chr1:181088466-181088704 | Rare:78 | ||||
chr1:182388840-182389062 | Common:3; Rare:46 | ||||
chr1:182390367-182390660 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
chr1:182391293-182391446 | Rare:31 | ||||
chr1:182391652-182392043 | Common:5; Rare:142; Clinvar:5; Clinvar (benign):5 | ||||
chr1:182789622-182789796 | Common:2; Rare:62 | ||||
chr1:183023043-183023285 | Common:5; Rare:63 | ||||
chr1:183472219-183472544 | Common:2; Rare:107 | ||||
chr1:183590886-183591064 | Common:3; Rare:34 | ||||
chr1:183635570-183636109 | Common:5; Rare:147 | ||||
chr1:183805001-183805268 | Rare:75 |