Variant report

Variant	rs10509598
Chromosome Location	chr10:92047571-92047572
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	chr10:92046589..92049031-chr10:92410934..92413664,2	MCF-7	breast:
2	chr10:92047473..92050346-chr10:92165247..92168101,3	MCF-7	breast:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10785952	0.96[ASN][1000 genomes]
rs12761749	0.96[ASN][1000 genomes]
rs12762226	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12762729	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12772587	0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12778542	0.96[ASN][1000 genomes]
rs12778920	0.96[ASN][1000 genomes]
rs12779366	1.00[ASN][1000 genomes]
rs12779831	1.00[ASN][1000 genomes]
rs12779981	0.96[ASN][1000 genomes]
rs12784961	0.91[ASN][1000 genomes]
rs1887183	0.96[ASN][1000 genomes]
rs1887184	0.96[ASN][1000 genomes]
rs1887185	0.96[ASN][1000 genomes]
rs1887186	0.96[ASN][1000 genomes]
rs2419666	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35440289	0.82[EUR][1000 genomes]
rs4994943	0.96[ASN][1000 genomes]
rs4994945	0.96[ASN][1000 genomes]
rs4994946	0.96[ASN][1000 genomes]
rs7087199	0.87[ASN][1000 genomes]
rs7896252	0.96[ASN][1000 genomes]
rs7905038	0.96[ASN][1000 genomes]
rs7907215	0.96[ASN][1000 genomes]
rs7919251	0.96[ASN][1000 genomes]
rs7919262	0.96[ASN][1000 genomes]
rs7922885	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895883	chr10:91610601-92195828	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1039731	chr10:91645718-92198264	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv540743	chr10:91645718-92198264	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv467430	chr10:91681344-92297943	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv551875	chr10:91681344-92297943	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	esv3375393	chr10:91880933-92243227	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	esv2422237	chr10:91940542-92547558	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr10:92041000-92048600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr10:92047000-92048200	Enhancers	Fetal Intestine Small	intestine

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