Variant report

Variant	rs11217622
Chromosome Location	chr11:119867937-119867938
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:119867354..119869206-chr11:119872754..119874804,2	K562	blood:
2	chr11:119853779..119856334-chr11:119866020..119869388,3	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11217619	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11217620	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11217621	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11217625	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11217627	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11822515	0.96[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs11825934	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11825954	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11828327	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12277627	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13377460	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13377464	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13377571	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58030968	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7106560	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7110709	0.88[YRI][hapmap];0.96[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs7119315	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7119397	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7119762	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7119865	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7119877	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7120110	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7125377	0.96[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs7125556	0.92[YRI][hapmap];0.96[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs73586071	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7924586	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7932064	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7937531	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7941864	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7945097	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7945351	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7945376	1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs7950202	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054057	chr11:119781953-120519770	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv541178	chr11:119781953-120519770	Weak transcription Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv832285	chr11:119789595-119957724	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1037777	chr11:119842515-119898368	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv541179	chr11:119842515-119898368	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1035918	chr11:119853069-119879255	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119860800-119869400	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr11:119862000-119871400	Weak transcription	Brain Germinal Matrix	brain
3	chr11:119864800-119871600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:119866400-119880200	Weak transcription	Esophagus	oesophagus
5	chr11:119866600-119868400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr11:119866600-119871600	Weak transcription	Brain Angular Gyrus	brain
7	chr11:119867000-119871200	Weak transcription	Brain Substantia Nigra	brain
8	chr11:119867600-119870600	Weak transcription	Brain Hippocampus Middle	brain
9	chr11:119867600-119871400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr11:119867600-119871400	Weak transcription	Brain Inferior Temporal Lobe	brain

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