Variant report

Variant	rs6928842
Chromosome Location	chr6:144395832-144395833
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13210804	1.00[ASN][1000 genomes]
rs1883447	0.94[ASN][1000 genomes]
rs28677011	0.99[ASN][1000 genomes]
rs34372511	0.99[ASN][1000 genomes]
rs35096948	0.96[ASN][1000 genomes]
rs35575158	0.99[ASN][1000 genomes]
rs35871914	0.99[ASN][1000 genomes]
rs35965932	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56195768	0.96[ASN][1000 genomes]
rs68151517	0.96[ASN][1000 genomes]
rs71564463	0.99[ASN][1000 genomes]
rs73008258	0.99[ASN][1000 genomes]
rs7752460	0.99[ASN][1000 genomes]
rs9496851	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9496856	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886738	chr6:144387698-144428387	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144386400-144408800	Weak transcription	Right Ventricle	heart
2	chr6:144388400-144396600	Weak transcription	K562	blood
3	chr6:144395000-144396600	Enhancers	GM12878-XiMat	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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