Variant report

Variant	rs6960513
Chromosome Location	chr7:47878907-47878908
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:47871874..47874312-chr7:47876088..47879038,2	K562	blood:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10245949	0.92[CEU][hapmap];0.82[CHB][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10280228	0.85[YRI][hapmap]
rs1074780	0.90[CHB][hapmap]
rs11769398	0.93[JPT][hapmap]
rs12670579	0.92[CEU][hapmap];0.82[CHB][hapmap]
rs13228166	0.90[CHB][hapmap];0.80[YRI][hapmap];0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs13237611	0.96[CEU][hapmap];0.90[CHB][hapmap];0.85[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1551275	0.96[CEU][hapmap];0.90[CHB][hapmap];0.85[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17659868	0.85[JPT][hapmap]
rs17710832	0.89[CEU][hapmap];0.82[CHB][hapmap]
rs17710874	0.93[JPT][hapmap]
rs1980279	0.92[CEU][hapmap];0.84[AMR][1000 genomes]
rs2123608	0.92[CEU][hapmap];0.81[CHB][hapmap]
rs2177164	0.89[CEU][hapmap];0.82[CHB][hapmap]
rs3757379	0.89[CEU][hapmap];0.86[CHB][hapmap];0.81[AMR][1000 genomes]
rs3800568	0.92[CEU][hapmap];0.82[CHB][hapmap];0.81[AMR][1000 genomes]
rs4543454	0.92[CEU][hapmap];0.82[CHB][hapmap];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4724647	0.90[CHB][hapmap]
rs6463451	0.86[CEU][hapmap]
rs6947216	0.92[CEU][hapmap];0.82[CHB][hapmap];0.81[AMR][1000 genomes]
rs6959021	0.85[JPT][hapmap]
rs6967514	0.85[CHB][hapmap];0.80[YRI][hapmap];0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs6968437	0.89[CEU][hapmap];0.85[CHB][hapmap]
rs6975745	0.96[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7777539	0.81[AMR][1000 genomes]
rs7783295	0.92[CEU][hapmap];0.82[CHB][hapmap]
rs7783894	0.89[CEU][hapmap];0.80[CHB][hapmap]
rs876467	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9639016	0.96[CEU][hapmap];0.90[CHB][hapmap];0.93[JPT][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9639987	0.96[CEU][hapmap];0.90[CHB][hapmap];0.93[JPT][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[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	nsv1026223	chr7:47560728-48243287	Genic enhancers Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv888003	chr7:47694270-47907214	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats 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 target site	5 gene(s)	inside rSNPs	diseases
3	nsv869585	chr7:47765428-48151324	Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv830991	chr7:47854530-48025996	Weak transcription Active TSS Genic enhancers Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:47852800-47879000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:47855000-47880200	Weak transcription	Lung	lung
3	chr7:47855800-47902400	Weak transcription	Adipose Nuclei	Adipose
4	chr7:47867200-47886000	Weak transcription	Right Atrium	heart
5	chr7:47867800-47886000	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr7:47868600-47879200	Weak transcription	Pancreas	Pancrea
7	chr7:47868800-47886000	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr7:47869800-47885400	Weak transcription	HSMMtube	muscle
9	chr7:47870000-47880200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr7:47877200-47880200	Weak transcription	Left Ventricle	heart
11	chr7:47877200-47882800	Weak transcription	Fetal Heart	heart
12	chr7:47877200-47884800	Weak transcription	Right Ventricle	heart
13	chr7:47878200-47879200	Weak transcription	Fetal Muscle Leg	muscle
14	chr7:47878400-47883800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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