Variant report

Variant	rs7531146
Chromosome Location	chr1:76851778-76851779
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11162131	1.00[EUR][1000 genomes]
rs11162132	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs12084205	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs12144245	1.00[EUR][1000 genomes]
rs12144641	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs12145151	1.00[CEU][hapmap]
rs1408867	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs60691804	1.00[EUR][1000 genomes]
rs6688662	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs73004234	1.00[EUR][1000 genomes]
rs73006116	1.00[EUR][1000 genomes]
rs73006118	1.00[EUR][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	nsv870621	chr1:76620313-76997071	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv534168	chr1:76718950-77039352	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1006776	chr1:76777323-76899975	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1014231	chr1:76781140-76880630	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv462006	chr1:76826279-77042405	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv546585	chr1:76826279-77042405	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76847600-76857600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr1:76851200-76851800	Enhancers	Rectal Smooth Muscle	rectum
3	chr1:76851200-76852200	Enhancers	Duodenum Mucosa	Duodenum
4	chr1:76851400-76852000	Enhancers	Fetal Intestine Small	intestine
5	chr1:76851400-76852400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:76851400-76852600	Enhancers	Fetal Heart	heart
7	chr1:76851400-76853000	Enhancers	Small Intestine	intestine

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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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