Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:181223422-181223721 | Common:3; Rare:77 | ||||
chr5:181261073-181261220 | Rare:43 | ||||
chr6:2245453-2245812 | Common:1; Rare:124 | ||||
chr6:4021213-4021415 | Rare:90 | ||||
chr6:5003640-5003864 | Common:5; Rare:75 | ||||
chr6:5004007-5004118 | Common:1; Rare:52 | ||||
chr6:5260730-5261025 | Common:2; Rare:93; Clinvar (benign):2 | ||||
chr6:7313088-7313234 | Common:4; Rare:65 | ||||
chr6:7389732-7389855 | Common:1; Rare:40 | ||||
chr6:8435326-8435689 | Common:5; Rare:125 | ||||
chr6:10694603-10694988 | Common:4; Rare:103 | ||||
chr6:10722839-10723237 | Common:6; Rare:136 | ||||
chr6:13615177-13615515 | Common:2; Rare:137 | ||||
chr6:16761456-16761726 | Common:2; Rare:84 | ||||
chr6:17706421-17706516 | Rare:40 |