Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21176852-21177153 | Common:1; Rare:88 | ||||
chr1:21345454-21345674 | Common:2; Rare:80 | ||||
chr1:21439939-21440158 | Common:2; Rare:48 | ||||
chr1:21783086-21783279 | Common:2; Rare:69 | ||||
chr1:23019285-23019503 | Rare:63 | ||||
chr1:23368290-23368523 | Common:1; Rare:60 | ||||
chr1:23368804-23368974 | Common:1; Rare:58 | ||||
chr1:23559474-23559643 | Common:1; Rare:71 | ||||
chr1:23778268-23778612 | Common:10; Rare:139 | ||||
chr1:23793535-23793657 | Rare:30 | ||||
chr1:23800729-23800984 | Common:1; Rare:93 | ||||
chr1:23825411-23825537 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23868252-23868438 | Common:6; Rare:61; Clinvar:2; Clinvar (benign):5 | ||||
chr1:23959670-23959916 | Common:2; Rare:59 | ||||
chr1:23980191-23980517 | Rare:86 |