Variant report

Variant	rs56123566
Chromosome Location	chr7:121204051-121204052
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs11982466	0.91[ASN][1000 genomes]
rs12113263	0.90[ASN][1000 genomes]
rs12538176	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1358498	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17132746	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17132749	0.91[ASN][1000 genomes]
rs17132759	0.90[ASN][1000 genomes]
rs17143490	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17143502	0.91[ASN][1000 genomes]
rs17143518	0.91[ASN][1000 genomes]
rs17143547	0.90[ASN][1000 genomes]
rs17143550	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1807810	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2049701	0.91[ASN][1000 genomes]
rs2214706	0.89[ASN][1000 genomes]
rs2214707	0.89[ASN][1000 genomes]
rs5000108	0.91[ASN][1000 genomes]
rs5000110	0.89[ASN][1000 genomes]
rs5000111	0.89[ASN][1000 genomes]
rs5000112	0.89[ASN][1000 genomes]
rs5000113	0.91[ASN][1000 genomes]
rs5000115	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5000116	0.91[ASN][1000 genomes]
rs55718335	0.91[ASN][1000 genomes]
rs55724857	0.92[ASN][1000 genomes]
rs55818559	0.90[ASN][1000 genomes]
rs55972921	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56156049	0.85[ASN][1000 genomes]
rs56377404	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56911184	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57704564	0.90[ASN][1000 genomes]
rs58109668	0.91[ASN][1000 genomes]
rs60537016	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60858294	0.94[ASN][1000 genomes]
rs62472521	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62472545	0.91[ASN][1000 genomes]
rs6466797	0.90[ASN][1000 genomes]
rs68030420	0.90[ASN][1000 genomes]
rs6942542	0.90[ASN][1000 genomes]
rs6944967	0.91[ASN][1000 genomes]
rs6946556	0.91[ASN][1000 genomes]
rs6947850	0.91[ASN][1000 genomes]
rs6962871	0.91[ASN][1000 genomes]
rs6963361	0.91[ASN][1000 genomes]
rs6967572	0.90[ASN][1000 genomes]
rs6967738	0.90[ASN][1000 genomes]
rs736411	0.91[ASN][1000 genomes]
rs736412	0.91[ASN][1000 genomes]
rs740100	0.90[ASN][1000 genomes]
rs757710	0.90[ASN][1000 genomes]
rs757711	0.91[ASN][1000 genomes]
rs757712	0.91[ASN][1000 genomes]
rs7778645	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7781058	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7798219	0.92[ASN][1000 genomes]
rs7798404	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7809871	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7810840	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032054	chr7:120926379-121432971	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv539103	chr7:120926379-121432971	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv608333	chr7:121132213-121379616	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1015438	chr7:121161554-121221761	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	esv2761362	chr7:121172202-121252112	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121203800-121216600	Weak transcription	H9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links