Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:14712947-14713233 | Rare:88; Clinvar (benign):2 | ||||
chr5:32092790-32092910 | Rare:20 | ||||
chr5:33161893-33162171 | Common:5; Rare:45 | ||||
chr5:43066972-43067066 | Rare:23 | ||||
chr5:43543085-43543367 | Common:2; Rare:78 | ||||
chr5:55944413-55944616 | Rare:46 | ||||
chr5:68275288-68275320 | Rare:10 | ||||
chr5:84382396-84382453 | Common:1; Rare:12 | ||||
chr5:96770328-96770554 | Common:1; Rare:40 | ||||
chr5:112160778-112160892 | Common:2; Rare:50 | ||||
chr5:128083053-128083160 | Common:2; Rare:31 | ||||
chr5:148826354-148826650 | Common:4; Rare:73 | ||||
chr5:148826888-148827189 | Common:2; Rare:78; Clinvar (benign):1 | ||||
chr5:148827387-148827919 | Common:2; Rare:128 | ||||
chr5:148834818-148834976 | Common:1; Rare:26 |