Variant report

Variant	rs7944185
Chromosome Location	chr11:16528586-16528587
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10832618	0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10832623	0.96[ASN][1000 genomes]
rs11023973	0.82[ASN][1000 genomes]
rs11023979	0.82[ASN][1000 genomes]
rs11023982	0.82[ASN][1000 genomes]
rs11512060	0.93[ASN][1000 genomes]
rs11529134	0.83[AMR][1000 genomes]
rs11529589	0.96[ASN][1000 genomes]
rs12146438	0.93[ASN][1000 genomes]
rs12362867	0.87[ASN][1000 genomes]
rs12363505	0.93[ASN][1000 genomes]
rs1354329	0.93[ASN][1000 genomes]
rs4576784	0.96[ASN][1000 genomes]
rs4622221	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4639898	0.81[AMR][1000 genomes]
rs56311489	0.93[ASN][1000 genomes]
rs67150549	0.96[ASN][1000 genomes]
rs72859415	0.82[ASN][1000 genomes]
rs72875213	0.82[ASN][1000 genomes]
rs72875217	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv553566	chr11:16329009-16799044	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv897016	chr11:16455794-16691743	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr11:16510400-16533000	Weak transcription	Fetal Heart	heart
2	chr11:16528000-16531400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr11:16528000-16533400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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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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