Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:151028956-151029252 | Common:2; Rare:49 | ||||
chr5:159100324-159100517 | Common:3; Rare:62 | ||||
chr5:160468092-160468252 | Rare:31 | ||||
chr5:170752286-170752543 | Common:4; Rare:55 | ||||
chr5:172381146-172381181 | Rare:10 | ||||
chr5:172452889-172452946 | Rare:10 | ||||
chr5:172656701-172656928 | Common:1; Rare:46 | ||||
chr5:173563312-173563509 | Common:2; Rare:38 | ||||
chr5:178206581-178206809 | Common:2; Rare:70 | ||||
chr5:179832744-179833061 | Common:6; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
chr5:180830844-180831027 | Common:1; Rare:58 | ||||
chr5:180831582-180831699 | Common:2; Rare:51 | ||||
chr5:181191822-181192083 | Common:3; Rare:83 | ||||
chr6:2989604-2989942 | Common:8; Rare:93 | ||||
chr6:3083004-3083187 | Rare:59 |