Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:51453013-51453388 | Rare:146 | ||||
chr13:51584409-51584522 | Common:1; Rare:45 | ||||
chr13:51804097-51804236 | Common:2; Rare:43 | ||||
chr13:52012162-52012421 | Common:2; Rare:85; Clinvar:1 | ||||
chr13:52455294-52455507 | Common:3; Rare:66 | ||||
chr13:52652590-52652916 | Common:3; Rare:101 | ||||
chr13:72727604-72727943 | Common:4; Rare:120 | ||||
chr13:72781859-72782198 | Common:1; Rare:133 | ||||
chr13:75549437-75549826 | Common:8; Rare:100 | ||||
chr13:76992047-76992188 | Common:1; Rare:66; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
chr13:77027136-77027295 | Common:5; Rare:52 | ||||
chr13:77918800-77918881 | Rare:17 | ||||
chr13:79405784-79405889 | Rare:39 | ||||
chr13:79406219-79406295 | Common:1; Rare:19 | ||||
chr13:94712534-94712662 | Common:1; Rare:30 |