Variant report

Variant	rs7776934
Chromosome Location	chr7:53020810-53020811
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11764198	0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs11764976	0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs34823614	0.92[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs59764082	0.97[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs66517709	0.82[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs73119609	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7781160	0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7781636	0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7781645	0.84[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7793897	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7794784	0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7799120	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7799263	0.84[AFR][1000 genomes];0.91[ASN][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	nsv888027	chr7:52588348-53190508	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1017676	chr7:52932139-53350524	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv831001	chr7:53003534-53152783	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv607008	chr7:53009355-53068819	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	inside rSNPs	diseases
5	nsv464449	chr7:53009493-53026365	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases
6	nsv607009	chr7:53009493-53026365	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:53016800-53023400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:53017200-53023400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr7:53017200-53026200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:53017200-53026800	Weak transcription	Fetal Heart	heart
5	chr7:53018400-53023400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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