Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154220451-154221016 | Common:1; Rare:189 | ||||
chr1:154272411-154272678 | Common:4; Rare:62; Clinvar:1; Clinvar (benign):3 | ||||
chr1:154501567-154501852 | Common:1; Rare:95 | ||||
chr1:154558884-154559089 | Common:1; Rare:70 | ||||
chr1:154585743-154585998 | Rare:57; Clinvar (benign):1 | ||||
chr1:154627875-154628018 | Common:3; Rare:76 | ||||
chr1:154868052-154868125 | Rare:11 | ||||
chr1:154870261-154870472 | Rare:44 | ||||
chr1:154936595-154936787 | Common:2; Rare:66 | ||||
chr1:154956067-154956232 | Common:1; Rare:46 | ||||
chr1:154961476-154961595 | Rare:36 | ||||
chr1:154961686-154962050 | Common:1; Rare:126 | ||||
chr1:154968769-154969072 | Rare:73 | ||||
chr1:154970040-154970358 | Common:1; Rare:95 | ||||
chr1:154970693-154970827 | Rare:28 |