Variant report

Variant	rs56868758
Chromosome Location	chr10:93286778-93286779
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93263800-93288000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:93272200-93296000	Weak transcription	HSMMtube	muscle
3	chr10:93278200-93296000	Weak transcription	HSMM	muscle
4	chr10:93278400-93298400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr10:93280800-93287600	Weak transcription	Psoas Muscle	Psoas
6	chr10:93285000-93287000	Enhancers	Fetal Lung	lung
7	chr10:93285000-93287000	Enhancers	Pancreas	Pancrea
8	chr10:93285400-93289200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr10:93286000-93287200	Flanking Active TSS	Liver	Liver
10	chr10:93286200-93287600	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr10:93286200-93287800	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr10:93286400-93288400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

Quick Search:

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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