Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:180802775-180802976 | Common:8; Rare:79 | ||||
chr5:180810081-180810200 | Common:2; Rare:31 | ||||
chr5:180861150-180861430 | Common:2; Rare:112 | ||||
chr5:181223112-181223328 | Rare:77 | ||||
chr5:181223526-181223749 | Common:4; Rare:53 | ||||
chr5:181243690-181243940 | Common:4; Rare:92 | ||||
chr5:181261065-181261272 | Rare:70 | ||||
chr6:292414-292537 | Rare:36 | ||||
chr6:2245453-2245784 | Common:1; Rare:115 | ||||
chr6:2971269-2971694 | Common:5; Rare:110 | ||||
chr6:3068496-3068563 | Common:1; Rare:14 | ||||
chr6:4021216-4021428 | Rare:97 | ||||
chr6:5003605-5003836 | Common:6; Rare:73 | ||||
chr6:5260677-5261013 | Common:3; Rare:115; Clinvar (benign):4 | ||||
chr6:5261263-5261553 | Common:9; Rare:72 |