Variant report

Variant	rs4477361
Chromosome Location	chr10:93421523-93421524
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11819558	0.96[ASN][1000 genomes]
rs11819574	0.96[ASN][1000 genomes]
rs17106864	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17106868	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17106892	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17106908	1.00[AMR][1000 genomes]
rs2242121	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs7069752	0.84[AMR][1000 genomes]
rs7071622	0.92[ASN][1000 genomes]
rs73320191	0.92[ASN][1000 genomes]
rs73322045	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73323911	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7907539	0.96[ASN][1000 genomes]
rs7914861	1.00[AMR][1000 genomes]
rs7915974	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93419200-93431400	Weak transcription	Psoas Muscle	Psoas
2	chr10:93420400-93424200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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

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