Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:51804121-51804272 | Common:2; Rare:44 | ||||
chr13:52012076-52012421 | Common:2; Rare:111; Clinvar:1 | ||||
chr13:52455229-52455503 | Common:3; Rare:84 | ||||
chr13:72727585-72727934 | Common:5; Rare:127 | ||||
chr13:72781853-72782188 | Common:1; Rare:130 | ||||
chr13:75549429-75549837 | Common:8; Rare:108 | ||||
chr13:76991946-76992160 | Common:3; Rare:106; Clinvar:20; Clinvar (benign):12 | ||||
chr13:77918800-77918881 | Rare:17 | ||||
chr13:79405792-79405880 | Rare:34 | ||||
chr13:95676916-95677238 | Common:4; Rare:117 | ||||
chr13:96053360-96053594 | Common:2; Rare:93 | ||||
chr13:99200667-99200894 | Common:6; Rare:104 | ||||
chr13:100088926-100089117 | Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596804-102597068 | Common:1; Rare:120; Clinvar (benign):1 | ||||
chr13:102773761-102773860 | Rare:39 |