Variant report

Variant	rs7137518
Chromosome Location	chr12:84122513-84122514
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1156936	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1304347	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17010967	1.00[AMR][1000 genomes]
rs17011014	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2036148	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2036149	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7136287	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73147867	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73147868	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73149738	0.96[ASN][1000 genomes]
rs73149739	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73149744	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73149792	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73151860	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73155681	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73161108	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73161109	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73161127	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73161137	0.96[ASN][1000 genomes]
rs73161140	0.96[ASN][1000 genomes]
rs73161141	0.96[ASN][1000 genomes]
rs73161142	0.96[ASN][1000 genomes]
rs73161144	0.96[ASN][1000 genomes]
rs73161147	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73161150	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73161152	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73161155	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7955659	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7962020	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7968087	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7979197	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7979696	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv559563	chr12:84017043-84450824	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv899355	chr12:84035467-84147295	Weak transcription ZNF genes & repeats Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1037138	chr12:84035912-84429867	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv541553	chr12:84035912-84429867	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1035818	chr12:84040289-84452115	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv559564	chr12:84042109-84441408	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1035252	chr12:84043334-84446432	ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv1041804	chr12:84050772-84466603	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1039889	chr12:84053336-84426064	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv541554	chr12:84053336-84426064	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv1049383	chr12:84062416-84290464	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv469497	chr12:84065324-84154003	Active TSS Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv559565	chr12:84065324-84154003	Enhancers ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3326179	chr12:84096533-84141528	ZNF genes & repeats Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv559566	chr12:84103615-84155936	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv899356	chr12:84103615-84213699	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv899357	chr12:84103615-84229254	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:84113200-84122600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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