Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:67226857-67227167 | Common:1; Rare:109 | ||||
chr16:67660222-67660373 | Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
chr16:67846713-67846968 | Common:1; Rare:69 | ||||
chr16:68023209-68023312 | Common:1; Rare:28 | ||||
chr16:68264430-68264534 | Rare:33 | ||||
chr16:68310928-68311019 | Rare:37 | ||||
chr16:69132547-69132663 | Rare:47 | ||||
chr16:69339548-69339799 | Rare:99; Clinvar (benign):1 | ||||
chr16:69726543-69726726 | Common:3; Rare:40 | ||||
chr16:70114136-70114369 | Common:3; Rare:83 | ||||
chr16:70346751-70346952 | Common:1; Rare:99 | ||||
chr16:70523538-70523837 | Common:3; Rare:93 | ||||
chr16:71895348-71895536 | Rare:55 | ||||
chr16:72093584-72093937 | Rare:88 | ||||
chr16:74296671-74296882 | Rare:82 |