Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:25233841-25234015 | Rare:71 | ||||
chr4:25376897-25377325 | Common:4; Rare:120 | ||||
chr4:25914051-25914291 | Common:2; Rare:103 | ||||
chr4:26320874-26321041 | Rare:56; Clinvar (benign):1 | ||||
chr4:26857579-26857776 | Common:2; Rare:66 | ||||
chr4:26860565-26860807 | Common:1; Rare:78 | ||||
chr4:37826579-37826729 | Common:1; Rare:55 | ||||
chr4:38664205-38664301 | Rare:35 | ||||
chr4:38867663-38867826 | Common:1; Rare:64 | ||||
chr4:39182250-39182548 | Rare:67; Clinvar:2 | ||||
chr4:39366302-39366456 | Common:1; Rare:47 | ||||
chr4:39458857-39459112 | Common:3; Rare:147; Clinvar (benign):5 | ||||
chr4:39527426-39527789 | Common:2; Rare:100 | ||||
chr4:39527951-39528070 | Rare:29 | ||||
chr4:39638817-39639140 | Common:1; Rare:116 |