Variant report

Variant	rs59059236
Chromosome Location	chr10:23660797-23660798
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23656800-23664800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr10:23657600-23660800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr10:23658400-23668000	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr10:23659600-23664400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr10:23660400-23661400	Weak transcription	HMEC	breast
6	chr10:23660600-23661600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr10:23660600-23662200	Weak transcription	NHEK	skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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