Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:106373788-106373887 | Rare:81 | ||||
chr14:106373895-106374259 | Rare:226 | ||||
chr14:106421795-106421963 | Common:9; Rare:133 | ||||
chr14:106538249-106538437 | Rare:82 | ||||
chr14:106578803-106578940 | Common:6; Rare:100 | ||||
chr14:106578966-106579075 | Common:5; Rare:74 | ||||
chr14:106592810-106593098 | Common:6; Rare:195 | ||||
chr14:106844749-106844885 | Rare:28 | ||||
chr15:22839446-22839668 | Rare:48 | ||||
chr15:29268692-29268749 | Common:2; Rare:14 | ||||
chr15:29268753-29268980 | Common:1; Rare:76; Clinvar (pathogenic):1 | ||||
chr15:31215471-31215663 | Common:3; Rare:36 | ||||
chr15:31223588-31223635 | Rare:19 | ||||
chr15:31345379-31345442 | Rare:16 | ||||
chr15:38670729-38670992 | Rare:46 |