Variant report

Variant	rs61834721
Chromosome Location	chr1:239630452-239630453
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10925903	0.92[ASN][1000 genomes]
rs10925906	0.92[ASN][1000 genomes]
rs11807305	0.92[ASN][1000 genomes]
rs12058126	0.92[ASN][1000 genomes]
rs12088138	0.92[ASN][1000 genomes]
rs12097468	0.89[ASN][1000 genomes]
rs12240097	0.92[ASN][1000 genomes]
rs16838358	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16838359	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16838363	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs20438	0.92[ASN][1000 genomes]
rs2354395	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2354400	0.90[EUR][1000 genomes]
rs58291256	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58463672	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58716948	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60374536	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61595023	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834689	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834709	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834710	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834711	0.85[EUR][1000 genomes]
rs61834712	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834713	0.85[EUR][1000 genomes]
rs61834714	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61834716	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834717	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834718	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834720	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834722	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834723	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6661441	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6666589	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6669508	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6675823	0.92[ASN][1000 genomes]
rs6681143	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6693126	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74149074	1.00[EUR][1000 genomes]
rs74149085	0.88[ASN][1000 genomes]
rs7513717	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7517458	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7519143	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7549234	0.92[ASN][1000 genomes]
rs7551209	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002301	chr1:239182255-239774393	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1006640	chr1:239290853-239658788	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv535358	chr1:239290853-239658788	Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv549435	chr1:239375010-239974006	Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	esv3373454	chr1:239495349-239670615	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv873350	chr1:239498915-239648140	Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv833037	chr1:239522168-239699412	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	esv3377526	chr1:239623743-240111639	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:239620400-239635800	Weak transcription	Gastric	stomach
2	chr1:239622400-239635200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr1:239623400-239633800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr1:239623400-239640800	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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