Variant report

Variant	rs62466356
Chromosome Location	chr7:101347666-101347667
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:101346607..101348692-chr7:101371323..101373114,2	MCF-7	breast:
2	chr7:101346109..101348713-chr7:101457175..101459861,2	MCF-7	breast:
3	chr7:101346602..101348960-chr7:101350465..101352401,2	MCF-7	breast:
4	chr7:101345813..101348514-chr7:101359172..101361201,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000257923	Chromatin interaction

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10239715	1.00[ASN][1000 genomes]
rs10269590	1.00[ASN][1000 genomes]
rs10270145	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10278430	0.80[AMR][1000 genomes]
rs10278534	1.00[ASN][1000 genomes]
rs10447812	1.00[ASN][1000 genomes]
rs11771998	0.84[AMR][1000 genomes]
rs11772618	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12667267	1.00[ASN][1000 genomes]
rs1619382	1.00[ASN][1000 genomes]
rs1636440	1.00[ASN][1000 genomes]
rs1636441	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1636442	0.82[AMR][1000 genomes]
rs1636443	1.00[ASN][1000 genomes]
rs1722218	1.00[ASN][1000 genomes]
rs1722224	1.00[ASN][1000 genomes]
rs1722226	1.00[ASN][1000 genomes]
rs1722229	1.00[ASN][1000 genomes]
rs2529183	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4263675	1.00[ASN][1000 genomes]
rs4276617	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4436052	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4490765	1.00[ASN][1000 genomes]
rs4535653	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4602818	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4642556	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4727503	1.00[ASN][1000 genomes]
rs4727504	1.00[ASN][1000 genomes]
rs4727505	1.00[ASN][1000 genomes]
rs4727506	1.00[ASN][1000 genomes]
rs4729747	1.00[ASN][1000 genomes]
rs56381219	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60702821	0.80[AMR][1000 genomes]
rs62463667	0.80[EUR][1000 genomes]
rs62463668	0.80[EUR][1000 genomes]
rs62463669	0.80[EUR][1000 genomes]
rs62463671	0.80[AMR][1000 genomes]
rs62463672	0.84[AMR][1000 genomes]
rs62463674	0.84[AMR][1000 genomes]
rs62463675	0.80[AMR][1000 genomes]
rs62463676	0.84[AMR][1000 genomes]
rs62463677	0.80[AMR][1000 genomes]
rs62466309	1.00[ASN][1000 genomes]
rs62466310	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62466312	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466343	1.00[ASN][1000 genomes]
rs62466344	1.00[ASN][1000 genomes]
rs62466345	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466346	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466347	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466348	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466349	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466350	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62466351	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466354	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466355	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466357	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466358	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467460	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467463	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467464	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467465	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467466	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467468	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467469	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6957219	1.00[ASN][1000 genomes]
rs6960571	1.00[ASN][1000 genomes]
rs757820	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs757821	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs757822	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs757823	1.00[ASN][1000 genomes]
rs757824	1.00[ASN][1000 genomes]
rs7785622	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7799319	1.00[ASN][1000 genomes]
rs7809926	1.00[ASN][1000 genomes]
rs7811421	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs848644	1.00[ASN][1000 genomes]
rs848645	1.00[ASN][1000 genomes]
rs848646	1.00[ASN][1000 genomes]
rs848654	1.00[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	nsv933653	chr7:100701931-101515782	Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv1018544	chr7:101225639-101424889	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv539045	chr7:101225639-101424889	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv482758	chr7:101231458-101395219	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv831079	chr7:101273495-101466776	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
6	nsv1021797	chr7:101342353-101466957	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv539046	chr7:101342353-101466957	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101332000-101376800	Weak transcription	Right Atrium	heart
2	chr7:101343400-101350000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:101345400-101350200	Weak transcription	Duodenum Mucosa	Duodenum
4	chr7:101345800-101350000	Weak transcription	Colonic Mucosa	Colon
5	chr7:101346200-101348600	Weak transcription	Stomach Mucosa	stomach
6	chr7:101346400-101349600	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr7:101346400-101350000	Weak transcription	Fetal Intestine Large	intestine
8	chr7:101346600-101348600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr7:101347400-101348200	Weak transcription	Rectal Mucosa Donor 31	rectum

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