Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:118591543-118591834 | Common:4; Rare:96 | ||||
chr4:119454554-119454904 | Common:16; Rare:118 | ||||
chr4:138928039-138928138 | Common:1; Rare:24 | ||||
chr4:138930062-138930270 | Common:4; Rare:49 | ||||
chr4:138931172-138931212 | Common:1; Rare:9 | ||||
chr4:140642023-140642076 | Rare:13 | ||||
chr4:140756852-140757132 | Rare:64 | ||||
chr4:151100730-151100989 | Rare:55 | ||||
chr4:153684096-153684337 | Common:1; Rare:74 | ||||
chr4:159102907-159103081 | Common:1; Rare:62 | ||||
chr4:168904844-168904993 | Common:3; Rare:22 | ||||
chr4:168924139-168924413 | Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
chr5:1633927-1634064 | Common:2; Rare:50 | ||||
chr5:2008385-2008499 | Common:2; Rare:30 | ||||
chr5:2756395-2756516 | Rare:40 |