Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:84768884-84768938 | Common:1; Rare:9 | ||||
chr6:84774803-84775016 | Common:1; Rare:55 | ||||
chr6:85404800-85405034 | Common:2; Rare:49 | ||||
chr6:85513814-85514079 | Rare:64; Clinvar (pathogenic):1 | ||||
chr6:85622380-85622623 | Common:1; Rare:34 | ||||
chr6:85677026-85677138 | Common:1; Rare:24 | ||||
chr6:85677795-85677856 | Rare:14 | ||||
chr6:85678405-85678631 | Common:3; Rare:57 | ||||
chr6:85678676-85678952 | Rare:107 | ||||
chr6:89158334-89158600 | Common:4; Rare:57 | ||||
chr6:89649138-89649202 | Rare:10 | ||||
chr6:100633213-100633380 | Common:1; Rare:33 | ||||
chr6:105546412-105546548 | Common:1; Rare:31 | ||||
chr6:106724901-106725164 | Common:1; Rare:54 | ||||
chr6:107375753-107375994 | Common:4; Rare:35 |