Variant report

Variant	rs6958697
Chromosome Location	chr7:119566164-119566165
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:119561524..119564382-chr7:119564905..119567041,3	K562	blood:
2	chr7:119558634..119561152-chr7:119564174..119567043,2	K562	blood:
3	chr7:119564930..119567525-chr7:119586667..119589307,3	K562	blood:

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10085666	0.89[EUR][1000 genomes]
rs10233853	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs10235983	0.89[EUR][1000 genomes]
rs10244657	0.89[EUR][1000 genomes]
rs10247975	0.89[EUR][1000 genomes]
rs10268381	0.89[EUR][1000 genomes]
rs10274212	0.89[EUR][1000 genomes]
rs10274517	0.89[EUR][1000 genomes]
rs10275081	0.89[EUR][1000 genomes]
rs10281584	0.89[EUR][1000 genomes]
rs1099822	0.89[EUR][1000 genomes]
rs12333906	0.89[EUR][1000 genomes]
rs12374758	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs1404081	0.89[EUR][1000 genomes]
rs1404082	0.89[EUR][1000 genomes]
rs1404084	0.89[EUR][1000 genomes]
rs1524200	0.89[EUR][1000 genomes]
rs1524201	0.89[EUR][1000 genomes]
rs1524204	0.89[EUR][1000 genomes]
rs1581503	0.89[EUR][1000 genomes]
rs1581505	0.89[EUR][1000 genomes]
rs1581506	0.89[EUR][1000 genomes]
rs1589753	0.89[EUR][1000 genomes]
rs1608584	0.89[EUR][1000 genomes]
rs1851807	0.89[EUR][1000 genomes]
rs1949782	0.89[EUR][1000 genomes]
rs1980321	0.89[EUR][1000 genomes]
rs2049378	0.82[EUR][1000 genomes]
rs2049380	0.89[EUR][1000 genomes]
rs2049382	0.89[EUR][1000 genomes]
rs2049383	0.89[EUR][1000 genomes]
rs2056583	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs2204310	0.89[EUR][1000 genomes]
rs2204311	0.89[EUR][1000 genomes]
rs2263403	0.89[EUR][1000 genomes]
rs2402489	0.89[EUR][1000 genomes]
rs28451901	0.89[EUR][1000 genomes]
rs4278103	0.89[EUR][1000 genomes]
rs4727902	0.89[EUR][1000 genomes]
rs58135787	0.89[EUR][1000 genomes]
rs58538319	0.89[EUR][1000 genomes]
rs58859180	0.89[EUR][1000 genomes]
rs6466712	0.89[EUR][1000 genomes]
rs6945733	0.89[EUR][1000 genomes]
rs6946613	0.84[YRI][hapmap]
rs6952445	0.89[EUR][1000 genomes]
rs6968560	0.89[EUR][1000 genomes]
rs73472916	0.89[EUR][1000 genomes]
rs73472917	0.89[EUR][1000 genomes]
rs73723022	0.86[AFR][1000 genomes]
rs7779237	0.89[EUR][1000 genomes]
rs7781144	0.89[EUR][1000 genomes]
rs7782751	0.89[EUR][1000 genomes]
rs7788783	0.89[EUR][1000 genomes]
rs7791400	0.89[EUR][1000 genomes]
rs7808015	0.89[EUR][1000 genomes]
rs846422	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs846423	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs846425	0.89[EUR][1000 genomes]
rs846426	0.89[EUR][1000 genomes]
rs846432	0.89[EUR][1000 genomes]
rs846433	0.89[EUR][1000 genomes]
rs846434	0.89[EUR][1000 genomes]
rs846435	0.89[EUR][1000 genomes]
rs846440	0.89[EUR][1000 genomes]
rs846442	0.89[EUR][1000 genomes]
rs846443	0.89[EUR][1000 genomes]
rs846449	0.89[EUR][1000 genomes]
rs9641626	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs9641627	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs9641628	0.89[EUR][1000 genomes]
rs9691446	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889115	chr7:119270386-119577292	ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1029023	chr7:119292763-119606632	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1023813	chr7:119292763-119606803	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv524225	chr7:119293417-119606632	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1029841	chr7:119299627-119606632	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1024175	chr7:119299627-119606803	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1028812	chr7:119310497-119604904	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv539097	chr7:119310497-119604904	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1033418	chr7:119324894-119600025	Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv539098	chr7:119324894-119600025	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv470388	chr7:119464310-119790102	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
12	nsv464706	chr7:119514703-119612541	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv608324	chr7:119514703-119612541	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	esv2753623	chr7:119532049-119770049	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:119565600-119566200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:119565600-119566400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:119565600-119566400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr7:119565800-119566400	Enhancers	Fetal Lung	lung
5	chr7:119566000-119566400	Flanking Active TSS	Fetal Brain Male	brain
6	chr7:119566000-119566400	Flanking Active TSS	K562	blood

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