Variant report

Variant	rs6563756
Chromosome Location	chr13:40397111-40397112
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs12865501	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12866856	0.82[CHD][hapmap]
rs1555629	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2209234	0.81[ASN][1000 genomes]
rs2324458	0.81[EUR][1000 genomes]
rs35023159	0.92[ASN][1000 genomes]
rs4379951	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4432144	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4447298	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4556674	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4575406	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4943703	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4943705	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61955567	0.92[ASN][1000 genomes]
rs6563757	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6563758	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6563764	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6563765	0.93[ASN][1000 genomes]
rs6563766	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6563768	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7323371	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7325743	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7336265	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7994425	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7997407	0.92[AFR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9285137	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9532443	0.88[ASN][1000 genomes]
rs9548943	0.88[ASN][1000 genomes]
rs9548944	0.96[ASN][1000 genomes]
rs9548945	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9576905	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9576907	0.81[ASN][1000 genomes]
rs9594373	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9603628	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054600	chr13:39801283-40545027	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1054797	chr13:40198744-40618428	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
3	nsv541755	chr13:40198744-40618428	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1040458	chr13:40249387-40638129	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6563756	C3orf57	trans	parietal	SCAN

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:40382600-40404000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr13:40392400-40408600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:40395000-40397600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr13:40395400-40397800	Enhancers	H9 Cell Line	embryonic stem cell
5	chr13:40395600-40397400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr13:40396000-40397200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr13:40396000-40397400	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr13:40396000-40397600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr13:40396000-40397800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr13:40396200-40397200	Enhancers	Primary T cells from cord blood	blood
11	chr13:40396200-40397400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr13:40396200-40397400	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr13:40396200-40397600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr13:40396200-40397800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr13:40396400-40397400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr13:40396600-40397200	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr13:40396600-40397400	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr13:40396600-40397400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr13:40396600-40397600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr13:40396600-40397600	Enhancers	HMEC	breast
21	chr13:40396600-40398000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr13:40396800-40397200	Enhancers	Primary T cells fromperipheralblood	blood
23	chr13:40396800-40397400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr13:40396800-40397800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr13:40396800-40397800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr13:40396800-40398000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr13:40397000-40397400	Enhancers	H1 Cell Line	embryonic stem cell

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