Variant report

Variant	rs17016797
Chromosome Location	chr2:35728866-35728867
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:33621149..33624012-chr2:35726795..35729641,2	MCF-7	breast:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10495841	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11124437	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11124438	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs11124446	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11682230	0.93[ASN][1000 genomes]
rs11688061	0.95[CHB][hapmap];0.94[JPT][hapmap];0.85[YRI][hapmap];0.93[ASN][1000 genomes]
rs11693441	0.93[ASN][1000 genomes]
rs11693497	0.91[ASN][1000 genomes]
rs11695142	0.86[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs12185690	0.96[ASN][1000 genomes]
rs17016746	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17016750	1.00[CEU][hapmap];0.88[YRI][hapmap];0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4313955	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4399704	0.97[ASN][1000 genomes]
rs4425057	0.88[JPT][hapmap];0.94[ASN][1000 genomes]
rs4619588	0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.97[ASN][1000 genomes]
rs5013113	0.88[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs5013114	0.88[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs5013115	0.89[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs5013116	0.88[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs5013117	0.89[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs5013118	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5013119	0.89[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs5013122	0.86[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs55728744	0.93[ASN][1000 genomes]
rs56001730	0.83[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs56051086	0.86[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs56053627	0.93[ASN][1000 genomes]
rs56235036	0.85[ASN][1000 genomes]
rs56305920	0.84[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs56665199	0.89[ASN][1000 genomes]
rs57242898	0.90[ASN][1000 genomes]
rs58358221	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6749401	0.97[ASN][1000 genomes]
rs72796501	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72796502	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7572867	0.80[EUR][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	nsv1010722	chr2:35072575-35950219	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv519522	chr2:35425529-35861883	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1008651	chr2:35469467-35896486	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
4	nsv999139	chr2:35483033-35860024	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
5	nsv535636	chr2:35483033-35860024	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
6	nsv873848	chr2:35641532-35973963	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
7	nsv949472	chr2:35709203-36447481	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv518450	chr2:35711861-35779358	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:35728000-35730000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:35728200-35730400	Enhancers	HMEC	breast
3	chr2:35728400-35729800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr2:35728400-35729800	Enhancers	Hela-S3	cervix
5	chr2:35728600-35729800	Enhancers	NHEK	skin
6	chr2:35728800-35729200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:35728800-35729200	Enhancers	HUVEC	blood vessel

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