Variant report

Variant	rs9370843
Chromosome Location	chr6:15914445-15914446
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11966220	0.83[AMR][1000 genomes]
rs34126499	0.83[AMR][1000 genomes]
rs34545176	0.83[AMR][1000 genomes]
rs35514893	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59691832	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9358074	0.87[ASN][1000 genomes]
rs9370839	0.87[ASN][1000 genomes]
rs9370841	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9383091	0.83[AMR][1000 genomes]
rs9396615	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15912600-15915800	Weak transcription	Left Ventricle	heart
2	chr6:15913000-15915600	Weak transcription	Fetal Heart	heart
3	chr6:15913600-15915800	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr6:15913600-15916800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:15913600-15920200	Weak transcription	Placenta	Placenta
6	chr6:15914000-15916400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr6:15914000-15921600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr6:15914200-15915600	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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