Variant report

Variant	rs8060282
Chromosome Location	chr16:82780866-82780867
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1000076	0.86[ASN][1000 genomes]
rs1000078	0.89[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs10514557	0.82[ASN][1000 genomes]
rs10514558	0.89[CHB][hapmap];0.81[JPT][hapmap];0.86[ASN][1000 genomes]
rs10514559	0.84[CHB][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs1157118	0.89[CHB][hapmap]
rs11646288	0.81[JPT][hapmap]
rs11646321	0.83[CHB][hapmap];0.82[ASN][1000 genomes]
rs11647530	0.82[ASN][1000 genomes]
rs1350888	0.83[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1350889	0.83[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs1462035	0.83[CHB][hapmap]
rs1462043	0.81[JPT][hapmap]
rs16958347	0.87[JPT][hapmap]
rs17183029	0.89[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs17183071	0.86[ASN][1000 genomes]
rs17183279	0.88[ASN][1000 genomes]
rs17183490	0.89[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs17273696	0.83[CHB][hapmap]
rs17274555	0.88[ASN][1000 genomes]
rs17274597	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17274793	0.87[ASN][1000 genomes]
rs17274905	0.88[ASN][1000 genomes]
rs1870843	0.80[JPT][hapmap]
rs2126369	0.88[ASN][1000 genomes]
rs2169447	0.82[JPT][hapmap]
rs2318186	0.86[ASN][1000 genomes]
rs2318187	0.88[ASN][1000 genomes]
rs4238723	0.81[JPT][hapmap]
rs4293370	0.84[ASN][1000 genomes]
rs4559899	0.93[JPT][hapmap]
rs4783262	0.81[ASN][1000 genomes]
rs4783263	0.81[JPT][hapmap]
rs4783266	0.81[JPT][hapmap]
rs55713633	0.83[ASN][1000 genomes]
rs58786779	0.85[ASN][1000 genomes]
rs62034479	0.81[ASN][1000 genomes]
rs62034480	0.82[ASN][1000 genomes]
rs62034481	0.82[ASN][1000 genomes]
rs62034482	0.82[ASN][1000 genomes]
rs62034484	0.83[ASN][1000 genomes]
rs7185447	0.86[ASN][1000 genomes]
rs7197336	0.88[CHB][hapmap];0.86[ASN][1000 genomes]
rs7197344	0.89[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs7197523	0.88[ASN][1000 genomes]
rs7201087	0.88[ASN][1000 genomes]
rs7201338	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8044955	0.81[JPT][hapmap]
rs8046067	0.85[ASN][1000 genomes]
rs8046098	0.89[CHB][hapmap];0.81[JPT][hapmap];0.88[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	nsv532599	chr16:82074439-82926863	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
2	nsv573367	chr16:82140561-83040846	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1057341	chr16:82363800-83198907	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
4	nsv542997	chr16:82363800-83198907	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1059718	chr16:82564054-82810003	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
6	nsv573379	chr16:82713551-82887631	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
7	esv2751616	chr16:82714696-82852296	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1067216	chr16:82719694-82821762	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
9	nsv543000	chr16:82719694-82821762	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
10	nsv1064438	chr16:82762729-82788901	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv907026	chr16:82765607-82812853	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv1066132	chr16:82769526-82847359	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv543001	chr16:82769526-82847359	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv573380	chr16:82770272-82781423	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82766800-82788600	Weak transcription	HMEC	breast
2	chr16:82768600-82784800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr16:82769200-82785200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr16:82770000-82782800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr16:82771000-82781000	Weak transcription	HSMMtube	muscle
6	chr16:82771000-82781400	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr16:82772400-82781000	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr16:82774200-82781400	Weak transcription	Aorta	Aorta
9	chr16:82774400-82792200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr16:82774600-82787400	Weak transcription	NHEK	skin
11	chr16:82775000-82781000	Weak transcription	HSMM	muscle
12	chr16:82780400-82781800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr16:82780400-82782000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr16:82780600-82781400	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr16:82780600-82781400	Enhancers	HUVEC	blood vessel
16	chr16:82780600-82781600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr16:82780600-82781800	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr16:82780600-82782000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr16:82780600-82782200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr16:82780800-82781000	Enhancers	HUES64 Cell Line	embryonic stem cell

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