Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:2245572-2245778 | Rare:69 | ||||
chr6:2765902-2765989 | Common:1; Rare:32 | ||||
chr6:2971533-2971864 | Common:1; Rare:86 | ||||
chr6:3456038-3456185 | Rare:46 | ||||
chr6:4021209-4021444 | Rare:106 | ||||
chr6:5003649-5003823 | Common:5; Rare:51 | ||||
chr6:5260691-5261070 | Common:6; Rare:134; Clinvar (benign):4 | ||||
chr6:7910777-7910899 | Rare:43 | ||||
chr6:8435421-8435646 | Common:3; Rare:79 | ||||
chr6:10412375-10412558 | Common:2; Rare:32 | ||||
chr6:10747630-10747806 | Common:2; Rare:68 | ||||
chr6:13328478-13328630 | Common:5; Rare:67 | ||||
chr6:13615159-13615515 | Common:3; Rare:143 | ||||
chr6:18122614-18122766 | Common:1; Rare:35; Clinvar (benign):2 | ||||
chr6:24666854-24667200 | Common:3; Rare:146 |