Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:53347525-53347699 | Common:1; Rare:47 | ||||
chr3:56557086-56557228 | Common:2; Rare:54 | ||||
chr3:57079269-57079375 | Common:2; Rare:38 | ||||
chr3:57227600-57227913 | Common:3; Rare:107 | ||||
chr3:57556009-57556321 | Rare:75 | ||||
chr3:57597290-57597778 | Common:4; Rare:143 | ||||
chr3:58433805-58433965 | Rare:63; Clinvar (benign):2 | ||||
chr3:62318888-62319062 | Rare:73 | ||||
chr3:63863743-63864158 | Common:8; Rare:138 | ||||
chr3:63864446-63864540 | Common:2; Rare:34 | ||||
chr3:67654583-67654712 | Common:1; Rare:45 | ||||
chr3:69013590-69013756 | Rare:44 | ||||
chr3:69052216-69052443 | Common:4; Rare:82 | ||||
chr3:69866217-69866284 | Rare:14 | ||||
chr3:71130539-71130685 | Rare:58; Clinvar:2 |