Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:31278043-31278369 | Common:2; Rare:69 | ||||
chr22:31620073-31620079 | |||||
chr22:32387926-32388224 | Common:4; Rare:84 | ||||
chr22:35312595-35312705 | Common:1; Rare:22 | ||||
chr22:35313902-35314108 | Rare:37 | ||||
chr22:35326987-35327375 | Common:1; Rare:93 | ||||
chr22:35849988-35850216 | Common:3; Rare:53 | ||||
chr22:36288725-36289301 | Common:2; Rare:174; Clinvar:6; Clinvar (benign):10 | ||||
chr22:36331419-36331637 | Common:2; Rare:40 | ||||
chr22:37806228-37806537 | Common:3; Rare:56 | ||||
chr22:37944989-37945042 | Rare:20 | ||||
chr22:38336103-38336319 | Rare:54 | ||||
chr22:38738257-38738357 | Rare:24 | ||||
chr22:38741492-38741760 | Common:1; Rare:55; Clinvar (benign):1 | ||||
chr22:41092881-41092931 | Rare:16 |