Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:140174919-140175275 | Common:1; Rare:104 | ||||
chr5:140564642-140564837 | Rare:56 | ||||
chr5:140647588-140647883 | Common:5; Rare:120; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140691317-140691641 | Common:1; Rare:111; Clinvar:8; Clinvar (benign):1 | ||||
chr5:141320732-141320864 | Common:2; Rare:42 | ||||
chr5:141636810-141637011 | Common:2; Rare:86 | ||||
chr5:141651353-141651483 | Rare:46 | ||||
chr5:141923721-141923910 | Common:1; Rare:56 | ||||
chr5:142324973-142325303 | Rare:108 | ||||
chr5:143404434-143404604 | Common:2; Rare:39 | ||||
chr5:144170546-144170816 | Common:1; Rare:88 | ||||
chr5:145937638-145937770 | Rare:32 | ||||
chr5:146182553-146182848 | Common:3; Rare:75 | ||||
chr5:148312358-148312441 | Common:1; Rare:20 | ||||
chr5:148383828-148384022 | Rare:57 |