Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:27251258-27251627 | Common:4; Rare:109 | ||||
chr13:27450104-27450232 | Common:3; Rare:41 | ||||
chr13:27450518-27450643 | Common:2; Rare:54 | ||||
chr13:27620443-27620737 | Common:2; Rare:97 | ||||
chr13:28658940-28659202 | Rare:111; Clinvar (pathogenic):1 | ||||
chr13:28718797-28719123 | Common:1; Rare:82 | ||||
chr13:30465795-30466069 | Common:1; Rare:96 | ||||
chr13:30617588-30617908 | Common:1; Rare:104 | ||||
chr13:33285703-33285887 | Rare:42 | ||||
chr13:33818011-33818197 | Common:1; Rare:80 | ||||
chr13:36346301-36346477 | Common:3; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
chr13:37869765-37869905 | Common:1; Rare:32 | ||||
chr13:38350215-38350390 | Rare:55 | ||||
chr13:39038079-39038460 | Common:1; Rare:91 | ||||
chr13:40982862-40983000 | Common:3; Rare:19 |