Variant report

Variant	rs11013615
Chromosome Location	chr10:18614236-18614237
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11013640	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11013723	0.91[ASN][1000 genomes]
rs12240995	1.00[JPT][hapmap]
rs17683651	1.00[JPT][hapmap]
rs2357929	1.00[JPT][hapmap]
rs4146986	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18602400-18614600	Weak transcription	Pancreas	Pancrea
2	chr10:18602600-18614600	Weak transcription	Ovary	ovary
3	chr10:18603000-18614800	Weak transcription	Aorta	Aorta
4	chr10:18613000-18614800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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