Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:45912085-45912216 | Common:2; Rare:31 | ||||
chr20:45934391-45934731 | Common:2; Rare:143 | ||||
chr20:45935053-45935400 | Common:1; Rare:139 | ||||
chr20:45972172-45972497 | Common:1; Rare:119 | ||||
chr20:46089863-46090070 | Rare:69 | ||||
chr20:46118160-46118330 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
chr20:46363962-46364099 | Common:1; Rare:29 | ||||
chr20:46364362-46364544 | Rare:69 | ||||
chr20:46406565-46406814 | Common:2; Rare:66 | ||||
chr20:47318384-47318587 | Rare:45 | ||||
chr20:47318703-47318921 | Common:1; Rare:68 | ||||
chr20:47318993-47319166 | Common:1; Rare:61 | ||||
chr20:47356657-47356888 | Rare:55 | ||||
chr20:47501736-47502019 | Common:1; Rare:100 | ||||
chr20:47786518-47786723 | Common:5; Rare:36 |