Variant report

Variant	rs10022049
Chromosome Location	chr4:91366628-91366629
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10019159	0.85[YRI][hapmap]
rs10024428	1.00[AFR][1000 genomes]
rs11930465	1.00[YRI][hapmap]
rs11944286	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs12331537	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs13435417	1.00[AFR][1000 genomes]
rs28421556	1.00[AFR][1000 genomes]
rs28447973	1.00[AFR][1000 genomes]
rs28472605	1.00[AFR][1000 genomes]
rs28479052	1.00[AFR][1000 genomes]
rs28479074	1.00[AFR][1000 genomes]
rs28643297	1.00[AFR][1000 genomes]
rs28781372	1.00[AFR][1000 genomes]
rs28866207	1.00[AFR][1000 genomes]
rs28887579	1.00[AFR][1000 genomes]
rs9993055	1.00[AFR][1000 genomes]
rs9994105	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9998060	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470053	chr4:90879613-91439573	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv931074	chr4:90970476-91753697	Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1007826	chr4:91049593-91438961	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv537177	chr4:91049593-91438961	Bivalent/Poised TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv999065	chr4:91049593-91520073	Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	esv1830936	chr4:91287204-91546380	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv534470	chr4:91342219-91842807	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr4:91361600-91368000	Enhancers	Hela-S3	cervix
2	chr4:91362800-91367200	Enhancers	HMEC	breast
3	chr4:91363000-91367200	Enhancers	NHEK	skin
4	chr4:91363000-91367400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:91364000-91366800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:91364200-91367200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:91364600-91367400	Enhancers	HUVEC	blood vessel

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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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