Variant report

Variant	rs7127264
Chromosome Location	chr11:84057164-84057165
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11820638	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs11821095	1.00[YRI][hapmap]
rs11821156	1.00[YRI][hapmap]
rs11821719	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs11822026	1.00[YRI][hapmap]
rs11828808	0.81[AFR][1000 genomes]
rs17147270	1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs17147287	1.00[YRI][hapmap]
rs56682848	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6592178	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7110833	0.89[YRI][hapmap]
rs7111176	1.00[YRI][hapmap]
rs7118527	1.00[YRI][hapmap]
rs7123236	1.00[YRI][hapmap]
rs7124855	1.00[YRI][hapmap]
rs7130145	0.85[AMR][1000 genomes]
rs7130835	1.00[YRI][hapmap]
rs7932078	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs7947801	1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948410	chr11:83918339-84812001	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1038641	chr11:83996453-84334045	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv541103	chr11:83996453-84334045	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1049696	chr11:84039547-84116297	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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