Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:140564278-140564458 | Common:2; Rare:56 | ||||
chr5:140564573-140564846 | Rare:75 | ||||
chr5:140647588-140647867 | Common:5; Rare:116; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140691260-140691452 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):1 | ||||
chr5:141320722-141320914 | Common:2; Rare:66 | ||||
chr5:142325014-142325225 | Rare:66 | ||||
chr5:148383880-148384027 | Rare:51 | ||||
chr5:149551360-149551624 | Rare:63 | ||||
chr5:154038879-154038993 | Common:1; Rare:36 | ||||
chr5:159207908-159207933 | Rare:8 | ||||
chr5:159263236-159263317 | Common:1; Rare:25 | ||||
chr5:160008918-160009177 | Common:1; Rare:51 | ||||
chr5:160419054-160419262 | Common:4; Rare:76 | ||||
chr5:172959181-172959460 | Common:4; Rare:74 | ||||
chr5:173328088-173328536 | Common:1; Rare:105 |