Variant report

Variant	rs9370853
Chromosome Location	chr6:15991331-15991332
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs4716020	0.95[CHB][hapmap];0.94[JPT][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67091502	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6940301	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs72653739	0.87[ASN][1000 genomes]
rs9349991	0.87[ASN][1000 genomes]
rs9367887	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9370849	0.85[CHB][hapmap]
rs9370851	0.87[ASN][1000 genomes]
rs9370852	0.86[ASN][1000 genomes]
rs9383097	0.82[ASN][1000 genomes]
rs9396623	0.85[CHB][hapmap];0.82[GIH][hapmap]
rs9396626	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9464841	0.89[CEU][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15988000-15995000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:15991200-15995000	Enhancers	K562	blood

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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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