Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:207053084-207053316 | Common:1; Rare:62 | ||||
chr1:207321751-207321831 | Rare:22 | ||||
chr1:207322104-207322138 | Rare:6 | ||||
chr1:207496075-207496252 | Rare:32 | ||||
chr1:207751945-207752144 | Common:1; Rare:63 | ||||
chr1:208244260-208244526 | Common:1; Rare:81 | ||||
chr1:209675225-209675470 | Common:2; Rare:59 | ||||
chr1:209937970-209938262 | Common:3; Rare:97; Clinvar (pathogenic):1 | ||||
chr1:211259750-211259995 | Rare:69 | ||||
chr1:211675579-211675792 | Common:1; Rare:42 | ||||
chr1:212035507-212035801 | Common:2; Rare:77 | ||||
chr1:212432793-212433090 | Rare:81 | ||||
chr1:212791672-212791945 | Common:6; Rare:127 | ||||
chr1:212858089-212858260 | Common:3; Rare:41 | ||||
chr1:214602930-214603276 | Common:3; Rare:97 |