Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:23641257-23641530 | Common:2; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
chr16:24729554-24729727 | Common:6; Rare:89 | ||||
chr16:25111521-25111855 | Common:2; Rare:105 | ||||
chr16:27268724-27268877 | Common:1; Rare:53 | ||||
chr16:27549868-27550161 | Common:2; Rare:109 | ||||
chr16:29961958-29962136 | Common:1; Rare:55 | ||||
chr16:29995610-29995698 | Rare:42 | ||||
chr16:29996072-29996296 | Common:2; Rare:79 | ||||
chr16:30065560-30065897 | Rare:114 | ||||
chr16:30075894-30076055 | Rare:55 | ||||
chr16:30123086-30123409 | Common:6; Rare:96 | ||||
chr16:30355219-30355431 | Common:1; Rare:74 | ||||
chr16:30534841-30535105 | Common:3; Rare:87 | ||||
chr16:30762063-30762325 | Common:3; Rare:89 | ||||
chr16:30787175-30787272 | Rare:11 |