Variant report

Variant	rs10881917
Chromosome Location	chr10:93295724-93295725
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10399998	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11186607	0.88[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs12259631	0.87[EUR][1000 genomes]
rs12259834	0.82[EUR][1000 genomes]
rs3904193	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3904194	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56826659	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[ASN][1000 genomes]

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93272200-93296000	Weak transcription	HSMMtube	muscle
2	chr10:93278200-93296000	Weak transcription	HSMM	muscle
3	chr10:93278400-93298400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr10:93288600-93296000	Weak transcription	Right Atrium	heart
5	chr10:93289400-93296000	Weak transcription	Liver	Liver
6	chr10:93289600-93296000	Weak transcription	Aorta	Aorta
7	chr10:93290000-93296000	Weak transcription	Pancreas	Pancrea
8	chr10:93290000-93296200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr10:93290800-93297000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr10:93295000-93296000	Weak transcription	Fetal Lung	lung
11	chr10:93295600-93297200	Enhancers	NHDF-Ad	bronchial

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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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