Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:44210705-44211084 | Common:5; Rare:140 | ||||
chr20:44531790-44531978 | Common:1; Rare:60 | ||||
chr20:44651687-44651789 | Common:1; Rare:31; Clinvar (benign):1 | ||||
chr20:44966391-44966560 | Rare:63 | ||||
chr20:45416035-45416158 | Rare:33 | ||||
chr20:45812306-45812708 | Common:4; Rare:113 | ||||
chr20:45857343-45857593 | Common:3; Rare:66 | ||||
chr20:46118140-46118330 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
chr20:47356678-47356887 | Rare:48 | ||||
chr20:47501744-47501993 | Common:1; Rare:87 | ||||
chr20:49046191-49046379 | Common:3; Rare:61 | ||||
chr20:49278036-49278278 | Rare:67 | ||||
chr20:50113127-50113292 | Common:6; Rare:72 | ||||
chr20:50153639-50153928 | Common:2; Rare:116 | ||||
chr20:50958478-50958853 | Common:1; Rare:133; Clinvar:1; Clinvar (benign):4 |