Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:36243859-36244142 | Common:2; Rare:62 | ||||
chr4:37826579-37826729 | Common:1; Rare:55 | ||||
chr4:37890992-37891257 | Common:3; Rare:82 | ||||
chr4:37977143-37977470 | Rare:85 | ||||
chr4:38664217-38664363 | Common:1; Rare:43 | ||||
chr4:38867516-38867833 | Common:2; Rare:95 | ||||
chr4:39045011-39045078 | Common:2; Rare:21 | ||||
chr4:39182202-39182548 | Rare:75; Clinvar:2 | ||||
chr4:39366319-39366416 | Rare:30 | ||||
chr4:39458884-39459122 | Common:2; Rare:131; Clinvar:1; Clinvar (benign):5 | ||||
chr4:39527337-39527761 | Common:4; Rare:107 | ||||
chr4:39527925-39528047 | Rare:30 | ||||
chr4:39638834-39639177 | Common:1; Rare:128 | ||||
chr4:39697936-39698203 | Common:2; Rare:116 | ||||
chr4:40629769-40629934 | Common:1; Rare:48 |