Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:3118587-3118750 | Common:2; Rare:56 | ||||
chr6:3157542-3157688 | Common:6; Rare:51 | ||||
chr6:4021218-4021422 | Rare:96 | ||||
chr6:5003610-5003823 | Common:6; Rare:62 | ||||
chr6:5004000-5004115 | Common:2; Rare:56 | ||||
chr6:5260723-5261009 | Common:2; Rare:91; Clinvar (benign):2 | ||||
chr6:7108414-7108656 | Common:1; Rare:76 | ||||
chr6:7313102-7313380 | Common:5; Rare:103 | ||||
chr6:7389740-7389881 | Common:1; Rare:41 | ||||
chr6:8435360-8435659 | Common:4; Rare:105 | ||||
chr6:10694614-10694976 | Common:4; Rare:92 | ||||
chr6:10747729-10747862 | Common:1; Rare:58 | ||||
chr6:11232590-11232825 | Rare:51 | ||||
chr6:12008733-12008771 | Rare:11 | ||||
chr6:12290108-12290361 | Rare:36 |