Variant report

Variant	rs7837296
Chromosome Location	chr8:42526894-42526895
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:42395559..42397564-chr8:42526201..42528579,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000168575	Chromatin interaction
ENSG00000176209	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10087172	0.83[JPT][hapmap]
rs10109429	0.83[JPT][hapmap]
rs1072003	0.83[JPT][hapmap]
rs10958725	0.84[ASN][1000 genomes]
rs10958727	0.98[ASN][1000 genomes]
rs13254578	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs13273442	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs13277254	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs13277524	0.98[ASN][1000 genomes]
rs13280301	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs13280604	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1451239	0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1451240	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1530847	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs16891561	0.88[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs1901281	0.95[ASN][1000 genomes]
rs1955185	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1955186	0.98[ASN][1000 genomes]
rs1979140	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2196128	0.83[JPT][hapmap]
rs2217732	0.83[JPT][hapmap]
rs2304297	0.83[JPT][hapmap]
rs34456987	0.80[ASN][1000 genomes]
rs34842664	0.81[ASN][1000 genomes]
rs35599391	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs36057318	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4236926	0.84[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs4295650	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4392883	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4736835	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4736838	0.82[ASN][1000 genomes]
rs4950	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4951	0.96[ASN][1000 genomes]
rs5005909	1.00[CEU][hapmap];0.89[JPT][hapmap]
rs55828312	0.89[ASN][1000 genomes]
rs57645595	0.88[ASN][1000 genomes]
rs58379124	0.81[ASN][1000 genomes]
rs6474411	0.81[ASN][1000 genomes]
rs6474412	0.88[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6474413	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6474414	0.96[ASN][1000 genomes]
rs6474415	0.96[ASN][1000 genomes]
rs6985052	0.98[ASN][1000 genomes]
rs6987704	0.98[ASN][1000 genomes]
rs6990603	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6997909	0.96[ASN][1000 genomes]
rs7004381	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7459838	0.89[ASN][1000 genomes]
rs7812298	0.83[JPT][hapmap]
rs7842601	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7845663	0.83[JPT][hapmap]
rs892413	0.83[JPT][hapmap]
rs9643853	0.98[ASN][1000 genomes]
rs9643891	0.98[ASN][1000 genomes]
rs9693825	0.95[ASN][1000 genomes]
rs9693858	0.93[ASN][1000 genomes]
rs9792257	0.98[ASN][1000 genomes]
rs9792277	0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530880	chr8:41895241-42755506	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1034724	chr8:42386707-42772203	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:42522200-42533400	Weak transcription	Dnd41	blood
2	chr8:42526800-42527200	Enhancers	Primary neutrophils fromperipheralblood	blood

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