Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:38350215-38350287 | Rare:37 | ||||
chr13:39038043-39038532 | Common:1; Rare:115 | ||||
chr13:39655628-39655838 | Common:3; Rare:102; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr13:40771125-40771377 | Common:3; Rare:82 | ||||
chr13:40982836-40983032 | Common:3; Rare:31 | ||||
chr13:41060121-41060528 | Common:3; Rare:143 | ||||
chr13:41060844-41061038 | Common:16; Rare:123 | ||||
chr13:41061144-41061598 | Common:4; Rare:153 | ||||
chr13:41061746-41061831 | Common:1; Rare:30 | ||||
chr13:41132715-41132997 | Rare:75 | ||||
chr13:41194351-41194652 | Common:2; Rare:72 | ||||
chr13:41457289-41457551 | Common:2; Rare:76 | ||||
chr13:42271777-42272190 | Common:4; Rare:109 | ||||
chr13:43023473-43023657 | Common:1; Rare:67 | ||||
chr13:43879458-43879676 | Common:1; Rare:55 |