Variant report

Variant	rs35770526
Chromosome Location	chr10:93284892-93284893
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs12775728	1.00[AMR][1000 genomes]
rs34718593	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35403049	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55908462	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61877880	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:14 , 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	chr10:93280200-93285600	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr10:93280200-93285600	Weak transcription	Spleen	Spleen
7	chr10:93280800-93285800	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr10:93280800-93287600	Weak transcription	Psoas Muscle	Psoas
9	chr10:93281600-93285200	Weak transcription	Liver	Liver
10	chr10:93281800-93285000	Weak transcription	Fetal Lung	lung
11	chr10:93281800-93285400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr10:93284200-93286400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr10:93284400-93285400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr10:93284600-93285000	Weak transcription	Pancreas	Pancrea

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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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