Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:3526201-3526453 | Common:3; Rare:58 | ||||
chr16:15719218-15719538 | Common:1; Rare:98; Clinvar:6; Clinvar (benign):3 | ||||
chr16:15719687-15719768 | Rare:30; Clinvar (benign):2 | ||||
chr16:15747872-15748108 | Common:4; Rare:69; Clinvar:5; Clinvar (benign):6 | ||||
chr16:15748110-15748214 | Common:2; Rare:24; Clinvar:4; Clinvar (benign):4 | ||||
chr16:15776076-15776382 | Common:2; Rare:69; Clinvar (benign):4 | ||||
chr16:19487891-19488182 | Common:3; Rare:54 | ||||
chr16:21820398-21820464 | Rare:14 | ||||
chr16:29139506-29139729 | Common:2; Rare:54 | ||||
chr16:29291064-29291096 | Common:1; Rare:6 | ||||
chr16:30634237-30634553 | Common:2; Rare:74 | ||||
chr16:30875333-30875471 | Rare:45 | ||||
chr16:30983728-30983942 | Rare:61 | ||||
chr16:67390307-67390586 | Common:1; Rare:86 | ||||
chr16:72664938-72665191 | Common:1; Rare:83 |