Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:30579941-30580228 | Common:1; Rare:51 | ||||
chr20:31604251-31604448 | Common:1; Rare:80 | ||||
chr20:33812311-33812477 | Rare:22 | ||||
chr20:34093717-34093903 | Rare:34 | ||||
chr20:34096659-34096938 | Rare:50 | ||||
chr20:35490957-35491074 | Rare:23 | ||||
chr20:36050286-36050746 | Common:2; Rare:156 | ||||
chr20:36122435-36122570 | Rare:20 | ||||
chr20:36606710-36607023 | Rare:73 | ||||
chr20:40619286-40619325 | Rare:4 | ||||
chr20:40687176-40687415 | Rare:41; Clinvar (benign):1 | ||||
chr20:40687634-40687803 | Rare:32; Clinvar:1; Clinvar (benign):2 | ||||
chr20:40687981-40688288 | Rare:67; Clinvar (benign):1 | ||||
chr20:41121727-41122067 | Common:1; Rare:86 | ||||
chr20:41412434-41412604 | Rare:31 |