Variant report

Variant	rs62439331
Chromosome Location	chr7:21587868-21587869
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10950861	0.88[EUR][1000 genomes]
rs11763790	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12667349	0.87[EUR][1000 genomes]
rs12668100	0.86[EUR][1000 genomes]
rs56356943	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56404110	0.87[EUR][1000 genomes]
rs60021305	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62439332	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62439333	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62439334	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62439335	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62439336	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62441662	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62441664	0.95[EUR][1000 genomes]
rs62441665	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62441666	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62441667	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62441668	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62441669	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62441670	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs62441672	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62441676	0.87[EUR][1000 genomes]
rs6461579	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6955340	0.94[EUR][1000 genomes]
rs6964528	0.87[EUR][1000 genomes]
rs6973537	0.94[EUR][1000 genomes]
rs6975155	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6976617	0.87[EUR][1000 genomes]
rs6977909	0.87[EUR][1000 genomes]
rs7788355	0.87[EUR][1000 genomes]
rs7789688	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7795069	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7801854	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7806515	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][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	nsv1027302	chr7:21391598-21727016	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv538800	chr7:21391598-21727016	Enhancers Genic enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1028434	chr7:21468437-21636671	ZNF genes & repeats Strong transcription Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv1023655	chr7:21486485-21727016	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv538801	chr7:21486485-21727016	ZNF genes & repeats Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	nsv830921	chr7:21489100-21688016	Strong transcription ZNF genes & repeats Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
7	nsv1030577	chr7:21548909-21681379	Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
8	nsv1025634	chr7:21566727-21686272	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv3520094	chr7:21587600-21587991	Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3520090	chr7:21587610-21587923	Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv3477138	chr7:21587615-21587905	Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3520091	chr7:21587615-21587942	Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3520092	chr7:21587649-21587878	Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv5289	chr7:21587676-21587968	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:21583600-21588400	Weak transcription	Pancreas	Pancrea
2	chr7:21583800-21591200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:21584000-21588200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr7:21584800-21590200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:21585200-21594400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr7:21585800-21590800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr7:21585800-21591000	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr7:21586000-21590600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr7:21586000-21591200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:21586000-21598800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr7:21586200-21590800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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