Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:121334450-121334579 | Common:3; Rare:51 | ||||
chr6:121435518-121435767 | Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
chr6:122471733-122471921 | Common:2; Rare:60 | ||||
chr6:122789171-122789343 | Common:1; Rare:44 | ||||
chr6:124962835-124962868 | Rare:13 | ||||
chr6:124963037-124963288 | Common:1; Rare:85 | ||||
chr6:125749413-125749762 | Common:5; Rare:138 | ||||
chr6:125781059-125781156 | Rare:18 | ||||
chr6:125986421-125986673 | Rare:106 | ||||
chr6:127118966-127119068 | Rare:17 | ||||
chr6:127266779-127266916 | Common:1; Rare:57 | ||||
chr6:127342377-127342560 | Common:1; Rare:32 | ||||
chr6:127343295-127343426 | Rare:28 | ||||
chr6:127343492-127343564 | Common:1; Rare:17 | ||||
chr6:127343567-127343609 | Common:1; Rare:12 |