Variant report

Variant	rs9319578
Chromosome Location	chr16:82936043-82936044
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs11150502	0.85[CHB][hapmap]
rs11150515	0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11150516	0.87[ASN][1000 genomes]
rs11150517	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11150518	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.89[MEX][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11862361	0.83[ASN][1000 genomes]
rs12716955	0.83[ASN][1000 genomes]
rs12928678	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs1559312	0.86[JPT][hapmap]
rs2059230	0.85[CHB][hapmap];0.88[JPT][hapmap]
rs2113140	0.85[CHB][hapmap]
rs2194287	0.87[ASN][1000 genomes]
rs2216739	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs4485358	0.85[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4513093	0.85[CHB][hapmap];0.80[MKK][hapmap]
rs4783293	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs4783294	0.85[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4783296	1.00[CHB][hapmap];0.94[CHD][hapmap];0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs6565075	0.85[CHB][hapmap]
rs7184056	0.85[CHB][hapmap]
rs7184177	0.84[CHD][hapmap]
rs7197619	0.84[CHD][hapmap]
rs7199677	0.84[CHD][hapmap]
rs7201088	0.85[CHB][hapmap]
rs7201829	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7498269	0.85[CHB][hapmap]
rs8052008	0.85[CHB][hapmap]
rs8052174	0.82[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs8053647	0.85[CHB][hapmap]
rs8063966	0.85[ASN][1000 genomes]
rs918660	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs918661	0.85[CHB][hapmap];0.82[CHD][hapmap];0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs929846	0.85[CHB][hapmap];0.88[JPT][hapmap]
rs929847	0.85[CHB][hapmap];0.88[JPT][hapmap]
rs929848	0.88[JPT][hapmap]
rs9319577	0.85[CHB][hapmap]
rs961283	0.86[CHB][hapmap]
rs9921828	0.85[CHB][hapmap]
rs9922147	0.93[ASN][1000 genomes]
rs9929316	0.91[ASN][1000 genomes]
rs9931196	0.85[CHB][hapmap]
rs9933935	0.85[CHB][hapmap]
rs9936039	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	nsv1063617	chr16:82786803-83229529	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2830385	chr16:82841335-82950413	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv573382	chr16:82905546-82950502	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82915800-82953000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr16:82926800-82961200	Weak transcription	HSMM	muscle
3	chr16:82933600-82940600	Weak transcription	Right Atrium	heart
4	chr16:82933800-82947000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr16:82934000-82947400	Weak transcription	Psoas Muscle	Psoas
6	chr16:82934000-83003400	Weak transcription	NHEK	skin
7	chr16:82934200-82952800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr16:82934400-82947200	Weak transcription	Left Ventricle	heart
9	chr16:82934400-82949200	Weak transcription	Aorta	Aorta
10	chr16:82934400-82967000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr16:82934400-82967400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr16:82934600-82989600	Weak transcription	HSMMtube	muscle
13	chr16:82934800-82938600	Weak transcription	HUVEC	blood vessel

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