Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:44251436-44252199 | Common:3; Rare:253 | ||||
chr6:53793662-53793800 | Common:2; Rare:25 | ||||
chr6:57961347-57961650 | Common:2; Rare:94 | ||||
chr6:73517847-73518268 | Common:2; Rare:113 | ||||
chr6:85678692-85678952 | Rare:99 | ||||
chr6:89721060-89721156 | Common:1; Rare:19 | ||||
chr6:106495149-106495279 | Common:1; Rare:19 | ||||
chr6:108589360-108589672 | Rare:68 | ||||
chr6:109454236-109454278 | Rare:12 | ||||
chr6:113650077-113650143 | Rare:15 | ||||
chr6:116277445-116277534 | Rare:15 | ||||
chr6:129427517-129427851 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr6:137868150-137868303 | Rare:29 | ||||
chr6:138032702-138032764 | Rare:9 | ||||
chr6:138035124-138035385 | Common:1; Rare:37 |