Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:44522011-44522213 | Common:2; Rare:64 | ||||
chr20:44651688-44651822 | Common:1; Rare:38; Clinvar (benign):1 | ||||
chr20:44885595-44885818 | Common:4; Rare:80 | ||||
chr20:44966351-44966566 | Common:1; Rare:86 | ||||
chr20:45306620-45306935 | Common:1; Rare:69 | ||||
chr20:45308297-45308328 | Rare:8 | ||||
chr20:45308778-45308865 | Common:1; Rare:17 | ||||
chr20:45313273-45313599 | Rare:92 | ||||
chr20:45406541-45406697 | Rare:41 | ||||
chr20:45791879-45791996 | Rare:45 | ||||
chr20:45834079-45834214 | Rare:52 | ||||
chr20:45857348-45857614 | Common:3; Rare:68 | ||||
chr20:45891206-45891387 | Common:1; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
chr20:45912146-45912273 | Common:3; Rare:31 | ||||
chr20:45934627-45934731 | Rare:54 |