Variant report

Variant	rs17026612
Chromosome Location	chr2:40967765-40967766
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs11124756	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11491284	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11689010	0.86[ASN][1000 genomes]
rs11887013	0.81[EUR][1000 genomes]
rs11899009	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12469563	0.85[ASN][1000 genomes]
rs12474948	0.85[EUR][1000 genomes]
rs12477643	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12712709	0.86[ASN][1000 genomes]
rs1541575	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17026319	0.85[EUR][1000 genomes]
rs17026434	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17026446	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17026537	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17026541	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17026544	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17026584	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17026616	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17026644	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1861307	0.81[ASN][1000 genomes]
rs1990617	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2005413	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2052260	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2160262	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2216043	0.86[ASN][1000 genomes]
rs2888699	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3911438	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs3915716	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs42787	0.85[EUR][1000 genomes]
rs4597578	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4610094	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4952643	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4952644	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs5022306	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56407568	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57225071	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57569001	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57770208	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs57955071	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57988012	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59892061	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs60373384	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61275311	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72945712	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7369946	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7369960	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7423585	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7581499	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873911	chr2:40423454-41161464	ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv873917	chr2:40710953-41015998	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv528865	chr2:40805427-41218810	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv873926	chr2:40835285-40986860	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv873927	chr2:40835285-41034225	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv470455	chr2:40835285-41059164	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv873928	chr2:40835285-41075134	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv873929	chr2:40835285-41180690	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv456441	chr2:40882402-41064824	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv581514	chr2:40882402-41064824	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv456452	chr2:40890416-40989061	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv581515	chr2:40890416-40989061	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv963911	chr2:40950223-40971701	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40949400-40973200	Weak transcription	HSMMtube	muscle
2	chr2:40963600-40968800	Weak transcription	HSMM	muscle
3	chr2:40964600-40968800	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr2:40967400-40968000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr2:40967600-40968000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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