Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:102827906-102828160 | Common:1; Rare:88 | ||||
chr4:102828182-102828291 | Common:2; Rare:31 | ||||
chr4:102868854-102869063 | Common:2; Rare:68 | ||||
chr4:103076302-103076338 | Rare:10 | ||||
chr4:105708628-105708827 | Rare:63 | ||||
chr4:106316191-106316601 | Common:5; Rare:132 | ||||
chr4:107989663-107990038 | Common:6; Rare:160; Clinvar:5; Clinvar (benign):5 | ||||
chr4:108620393-108620640 | Common:6; Rare:123 | ||||
chr4:109730057-109730242 | Common:2; Rare:45 | ||||
chr4:109815484-109815786 | Common:1; Rare:82 | ||||
chr4:110622738-110622917 | Common:3; Rare:36 | ||||
chr4:110623067-110623296 | Common:1; Rare:53 | ||||
chr4:112232148-112232246 | Rare:41 | ||||
chr4:112636885-112637199 | Common:1; Rare:86 | ||||
chr4:112637390-112637571 | Common:3; Rare:47 |