Variant report

Variant	rs7767864
Chromosome Location	chr6:118696338-118696339
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10456917	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10457330	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10457331	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10457335	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10457337	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10457338	0.85[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11153732	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11153734	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11153748	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11153752	0.86[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap];0.83[EUR][1000 genomes]
rs11153753	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11752626	0.82[CHB][hapmap]
rs11755121	0.86[CEU][hapmap];0.82[CHB][hapmap];0.93[JPT][hapmap];0.83[EUR][1000 genomes]
rs12192964	0.83[ASN][1000 genomes]
rs12194555	0.85[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12199463	0.85[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap];0.83[EUR][1000 genomes]
rs12205899	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12206329	0.86[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap];0.80[EUR][1000 genomes]
rs12214483	0.86[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12660455	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12661338	0.82[CHB][hapmap]
rs12665409	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13192336	0.85[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap]
rs13219555	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1344178	0.80[ASN][1000 genomes]
rs2077162	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2078079	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2078383	0.80[ASN][1000 genomes]
rs2213856	0.86[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2213857	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2356183	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2356492	0.86[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28655926	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34479834	0.83[EUR][1000 genomes]
rs35730412	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3734381	0.85[CEU][hapmap];0.93[JPT][hapmap]
rs3752581	0.86[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap]
rs3798420	0.85[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3890198	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3951042	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3951043	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4027880	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4307206	0.81[CHB][hapmap]
rs56403768	0.92[ASN][1000 genomes]
rs57813349	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57912492	0.92[ASN][1000 genomes]
rs6569013	0.84[ASN][1000 genomes]
rs6569014	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6569015	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6569017	0.80[ASN][1000 genomes]
rs6569020	0.86[CHB][hapmap];0.84[JPT][hapmap];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67832971	0.83[EUR][1000 genomes]
rs6903459	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6920640	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6925641	0.85[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap];0.83[EUR][1000 genomes]
rs6928210	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6936178	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7453914	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs763254	0.81[CHB][hapmap]
rs7746778	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7751467	0.83[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap]
rs7757815	0.80[ASN][1000 genomes]
rs7757943	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7764272	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7764280	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7772214	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9320648	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9320649	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9320650	0.80[ASN][1000 genomes]
rs9489355	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs973944	0.81[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530526	chr6:118027339-118718476	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv532051	chr6:118551027-119044197	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1020463	chr6:118593028-119146363	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv604554	chr6:118631282-118716318	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv830787	chr6:118631902-118805106	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1025403	chr6:118635123-119122551	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv1025456	chr6:118669672-119058789	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv1027444	chr6:118687556-119121660	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	nsv538428	chr6:118687556-119121660	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
10	nsv949321	chr6:118692304-119137658	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
11	nsv432958	chr6:118692307-119010307	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
12	nsv604555	chr6:118695049-118856822	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118688200-118700200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:118691400-118700400	Enhancers	Fetal Heart	heart
3	chr6:118692200-118699000	Weak transcription	Psoas Muscle	Psoas
4	chr6:118694200-118699600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr6:118694800-118698200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr6:118696000-118698200	Weak transcription	Left Ventricle	heart
7	chr6:118696200-118698200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr6:118696200-118699000	Weak transcription	Right Atrium	heart

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