Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:79988376-79988623 | Common:2; Rare:94 | ||||
chr19:572322-572603 | Rare:139 | ||||
chr19:633517-633720 | Common:8; Rare:97 | ||||
chr19:1103801-1104104 | Common:4; Rare:127 | ||||
chr19:1275772-1276131 | Common:2; Rare:159 | ||||
chr19:2096221-2096412 | Rare:66 | ||||
chr19:2269435-2269679 | Common:2; Rare:111 | ||||
chr19:2328542-2328696 | Rare:75 | ||||
chr19:3572661-3572991 | Common:1; Rare:93 | ||||
chr19:3981990-3982247 | Common:1; Rare:111; Clinvar (benign):2 | ||||
chr19:5293222-5293444 | Common:1; Rare:95 | ||||
chr19:5622765-5623144 | Common:5; Rare:134 | ||||
chr19:5680458-5680771 | Rare:94 | ||||
chr19:5978083-5978390 | Common:3; Rare:115 | ||||
chr19:7069663-7069735 | Common:1; Rare:21 |