Variant report

Variant	rs34349239
Chromosome Location	chr7:66846041-66846042
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:66840245..66841805-chr7:66844948..66846496,2	MCF-7	breast:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10085684	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10227991	0.81[EUR][1000 genomes]
rs10242530	0.81[EUR][1000 genomes]
rs10278852	0.81[EUR][1000 genomes]
rs10280504	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11975662	0.85[ASN][1000 genomes]
rs12673116	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12698580	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13438181	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2075082	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28542443	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28718590	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4521652	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6945404	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6957404	0.90[ASN][1000 genomes]
rs6957846	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73135830	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73148486	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73150465	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73150492	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73150498	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73152206	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7779003	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7789199	0.81[EUR][1000 genomes]
rs9654869	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758118	chr7:66401430-66859253	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	esv2759535	chr7:66401430-66859253	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv888330	chr7:66502171-66877880	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
4	nsv1031560	chr7:66805244-66846663	Enhancers Strong transcription Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1022779	chr7:66805244-66849392	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1031147	chr7:66811313-66922350	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1025049	chr7:66823977-66906930	Bivalent Enhancer Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	esv3374929	chr7:66843317-66848115	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv33458	chr7:66843998-66849444	Enhancers Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3430927	chr7:66844117-66847215	Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3342206	chr7:66844217-66847215	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:66843000-66847200	Enhancers	Fetal Stomach	stomach
2	chr7:66845200-66846200	Enhancers	Gastric	stomach
3	chr7:66845400-66846200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:66845600-66846200	Active TSS	Fetal Kidney	kidney

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