Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:82366041-82366068 | Rare:1 | ||||
chr4:82428516-82428550 | Rare:7 | ||||
chr4:82495903-82496042 | Rare:26 | ||||
chr4:83051849-83051871 | Rare:1 | ||||
chr4:88046505-88046913 | Common:2; Rare:111; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
chr4:88097328-88097578 | Common:2; Rare:61 | ||||
chr4:94410733-94411039 | Common:1; Rare:63 | ||||
chr4:94653912-94654461 | Common:3; Rare:100 | ||||
chr4:94759144-94759448 | Common:2; Rare:55 | ||||
chr4:94759468-94759765 | Common:3; Rare:47 | ||||
chr4:95159050-95159112 | Rare:13 | ||||
chr4:98900789-98901134 | Common:4; Rare:57 | ||||
chr4:101174087-101174389 | Common:4; Rare:63 | ||||
chr4:101279596-101279720 | Rare:22 | ||||
chr4:105682374-105682722 | Common:2; Rare:57 |