Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:103076307-103076385 | Rare:23 | ||||
chr4:105552305-105552650 | Rare:50 | ||||
chr4:105708636-105708827 | Rare:61 | ||||
chr4:106316173-106316601 | Common:5; Rare:136 | ||||
chr4:107824597-107824735 | Rare:30 | ||||
chr4:107989686-107989935 | Common:5; Rare:113; Clinvar:4; Clinvar (benign):5 | ||||
chr4:108620378-108620647 | Common:6; Rare:137 | ||||
chr4:109433756-109433938 | Common:1; Rare:60 | ||||
chr4:112232111-112232276 | Common:1; Rare:72 | ||||
chr4:112285801-112285966 | Rare:50 | ||||
chr4:112636885-112637187 | Common:1; Rare:84 | ||||
chr4:112637390-112637570 | Common:3; Rare:47 | ||||
chr4:112817999-112818245 | Rare:37 | ||||
chr4:113979582-113979708 | Common:1; Rare:30 | ||||
chr4:114598631-114598952 | Common:10; Rare:88 |