Variant report

Variant	rs11922703
Chromosome Location	chr3:156169211-156169212
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11922769	0.98[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs16826198	0.85[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs16826199	0.85[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs3755631	0.92[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs55671429	0.83[ASN][1000 genomes]
rs55754142	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs55754499	0.84[AFR][1000 genomes]
rs56261626	0.87[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs6789361	0.98[ASN][1000 genomes]
rs73873379	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73873383	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	nsv1014755	chr3:155889430-156411894	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:156162200-156169400	Weak transcription	Aorta	Aorta
2	chr3:156162600-156174800	Weak transcription	Brain Hippocampus Middle	brain
3	chr3:156167600-156169600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr3:156168200-156170200	Enhancers	Stomach Smooth Muscle	stomach
5	chr3:156168800-156170200	Enhancers	Rectal Smooth Muscle	rectum
6	chr3:156169000-156170400	Enhancers	Colon Smooth Muscle	Colon
7	chr3:156169200-156170000	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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