Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:58989911-58990327 | Common:3; Rare:87; Clinvar (benign):1 | ||||
chr5:58991769-58991852 | Common:1; Rare:14 | ||||
chr5:59004113-59004390 | Common:2; Rare:47 | ||||
chr5:59016300-59016476 | Common:8; Rare:30 | ||||
chr5:59019050-59019145 | Rare:13 | ||||
chr5:59033077-59033371 | Rare:40 | ||||
chr5:59034127-59034395 | Rare:54 | ||||
chr5:59037767-59038032 | Common:6; Rare:54 | ||||
chr5:59038116-59038415 | Rare:54 | ||||
chr5:59055658-59055927 | Common:2; Rare:46 | ||||
chr5:59066716-59066805 | Rare:16 | ||||
chr5:59066812-59066833 | Rare:2 | ||||
chr5:59074468-59074668 | Common:1; Rare:33 | ||||
chr5:59078349-59078405 | Common:1; Rare:7 | ||||
chr5:59078449-59078464 | Rare:1 |