Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:6708288-6708703 | Common:3; Rare:187 | ||||
chr8:9150615-9150826 | Common:1; Rare:69 | ||||
chr8:10839799-10839996 | Rare:82 | ||||
chr8:11284741-11284861 | Common:2; Rare:54 | ||||
chr8:11802419-11802806 | Common:6; Rare:217 | ||||
chr8:11847803-11848073 | Common:6; Rare:139; Clinvar (benign):1 | ||||
chr8:13133193-13133575 | Common:14; Rare:111 | ||||
chr8:13566745-13566905 | Common:6; Rare:57 | ||||
chr8:15540167-15540508 | Common:4; Rare:136; Clinvar:12; Clinvar (benign):1 | ||||
chr8:16567392-16567642 | Rare:58 | ||||
chr8:17246589-17247063 | Common:5; Rare:198 | ||||
chr8:17651770-17651891 | Rare:32 | ||||
chr8:17676345-17676447 | Common:3; Rare:31 | ||||
chr8:17676471-17676537 | Rare:18 | ||||
chr8:17692197-17692396 | Common:1; Rare:60 |