Variant report

Variant	rs35612403
Chromosome Location	chr7:12331980-12331981
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	chr7:12106833..12107747-chr7:12331137..12332178,5	MCF-7	breast:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10215270	0.88[ASN][1000 genomes]
rs10225682	0.97[AFR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10227871	0.85[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs10228123	0.81[ASN][1000 genomes]
rs10230889	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10240547	0.86[AFR][1000 genomes]
rs10256397	0.96[ASN][1000 genomes]
rs10259305	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10262667	0.90[ASN][1000 genomes]
rs10264702	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10268302	0.94[ASN][1000 genomes]
rs10268480	0.96[ASN][1000 genomes]
rs10272812	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1079506	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1117386	0.99[AFR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11971413	0.99[AFR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11980307	0.96[ASN][1000 genomes]
rs13437654	0.99[AFR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17165803	0.81[ASN][1000 genomes]
rs2287067	0.94[ASN][1000 genomes]
rs28722991	0.82[ASN][1000 genomes]
rs3899335	0.93[AFR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6460920	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6944872	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6948209	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6948366	0.94[ASN][1000 genomes]
rs6949574	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6967342	0.96[ASN][1000 genomes]
rs6971849	0.96[ASN][1000 genomes]
rs72584556	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72584589	0.97[ASN][1000 genomes]
rs72586705	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72586714	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72586729	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7800823	0.94[ASN][1000 genomes]
rs984568	0.96[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	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv534432	chr7:12148960-12693032	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv1024554	chr7:12214722-12967418	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv538735	chr7:12214722-12967418	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
5	nsv1033704	chr7:12286225-12355773	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv887629	chr7:12304555-12400837	ZNF genes & repeats Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1019021	chr7:12310445-12375516	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv887630	chr7:12323757-12400837	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12331400-12332400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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