Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:74292633-74292672 | Common:1; Rare:9 | ||||
chr12:106138792-106139113 | Rare:83 | ||||
chr12:124389351-124389444 | Rare:20 | ||||
chr12:130875654-130875989 | Common:2; Rare:69 | ||||
chr13:23888720-23888877 | Common:1; Rare:41 | ||||
chr13:29849516-29849544 | Rare:7 | ||||
chr13:29849631-29849959 | Rare:64 | ||||
chr13:110424831-110424961 | Common:4; Rare:48; Clinvar:3; Clinvar (benign):2 | ||||
chr13:110870201-110870550 | Common:3; Rare:56 | ||||
chr13:113928831-113929075 | Common:1; Rare:42 | ||||
chr14:22771061-22771347 | Common:2; Rare:100 | ||||
chr14:34874103-34874193 | Rare:24 | ||||
chr14:49622760-49622872 | Rare:27 | ||||
chr14:77027809-77027947 | Rare:66 | ||||
chr14:105093927-105094052 | Rare:30 |