Variant report

Variant	rs1345933
Chromosome Location	chr2:186337915-186337916
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10186680	1.00[EUR][1000 genomes]
rs10195783	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10803986	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10803987	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10803989	1.00[EUR][1000 genomes]
rs10931177	0.82[ASN][1000 genomes]
rs10931179	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1116602	1.00[EUR][1000 genomes]
rs11673741	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11887570	1.00[EUR][1000 genomes]
rs11900568	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12620350	1.00[EUR][1000 genomes]
rs12693410	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12693412	1.00[EUR][1000 genomes]
rs13002717	1.00[EUR][1000 genomes]
rs13015569	1.00[ASN][1000 genomes]
rs1424525	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1424526	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1424527	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1424538	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1477455	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1477457	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2193614	1.00[EUR][1000 genomes]
rs2194508	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2370391	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2370472	1.00[EUR][1000 genomes]
rs35336042	0.89[ASN][1000 genomes]
rs4265972	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4499391	1.00[EUR][1000 genomes]
rs4575687	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6434130	0.97[ASN][1000 genomes]
rs6706525	1.00[EUR][1000 genomes]
rs6713566	1.00[EUR][1000 genomes]
rs6752582	0.95[ASN][1000 genomes]
rs6761586	1.00[EUR][1000 genomes]
rs7567961	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7576818	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7602278	1.00[EUR][1000 genomes]
rs7606681	1.00[EUR][1000 genomes]
rs763329	1.00[EUR][1000 genomes]
rs991327	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv584009	chr2:186203397-186345148	Active TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv459982	chr2:186213755-186475590	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv584012	chr2:186213755-186475590	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv875525	chr2:186223503-186434458	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv459983	chr2:186245653-186377253	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv584013	chr2:186245653-186377253	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv875526	chr2:186272059-186434458	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv875527	chr2:186272059-186475590	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv459985	chr2:186293335-186422662	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv584014	chr2:186293335-186422662	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv459986	chr2:186297074-186413124	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv584015	chr2:186297074-186413124	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv584016	chr2:186301351-186410869	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv875528	chr2:186301351-186475590	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
15	nsv1004048	chr2:186303297-186541503	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	nsv875529	chr2:186303530-186434458	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
17	nsv875530	chr2:186303530-186475590	ZNF genes & repeats Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
18	nsv875531	chr2:186303530-186489537	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
19	nsv1009994	chr2:186308867-186370097	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
20	nsv997498	chr2:186308867-186391490	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
21	nsv875532	chr2:186309738-186422662	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
22	nsv875533	chr2:186309738-186433551	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
23	nsv875535	chr2:186309738-186458903	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
24	nsv875534	chr2:186309738-186475590	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
25	nsv875536	chr2:186309738-186504175	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
26	nsv875537	chr2:186336529-186422662	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186314400-186345200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:186321400-186358600	Weak transcription	HMEC	breast
3	chr2:186331800-186342000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:186332600-186340800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr2:186336200-186340800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr2:186337400-186338800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr2:186337400-186339200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:186337400-186339200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:186337400-186340800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr2:186337600-186338600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr2:186337600-186339000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:186337600-186340600	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr2:186337800-186340800	Weak transcription	H9 Cell Line	embryonic stem cell

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