Variant report

Variant	rs17674527
Chromosome Location	chr16:82929013-82929014
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11150522	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11150523	0.87[ASN][1000 genomes]
rs11649390	0.83[AMR][1000 genomes]
rs11863075	0.83[EUR][1000 genomes]
rs12919606	0.87[ASN][1000 genomes]
rs12923557	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs13331478	0.87[ASN][1000 genomes]
rs16958781	0.80[YRI][hapmap]
rs16958850	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs16958852	1.00[JPT][hapmap]
rs16958858	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs17675094	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs17741493	0.80[YRI][hapmap]
rs1991026	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1991028	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs28417188	0.87[ASN][1000 genomes]
rs28661446	0.87[ASN][1000 genomes]
rs34482883	0.87[ASN][1000 genomes]
rs35775260	0.87[ASN][1000 genomes]
rs4782737	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs4783299	0.87[ASN][1000 genomes]
rs4783300	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs62035221	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs62035222	0.87[AMR][1000 genomes]
rs6565078	0.88[CEU][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7187633	0.91[ASN][1000 genomes]
rs7190538	1.00[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7192482	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7205339	0.84[CEU][hapmap]
rs72790111	0.87[AMR][1000 genomes]
rs8045708	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs9926654	0.87[ASN][1000 genomes]
rs9930233	1.00[JPT][hapmap]
rs9936335	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs9940251	1.00[JPT][hapmap]
rs9941327	1.00[JPT][hapmap];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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
7	nsv1064158	chr16:82919690-82935671	Weak transcription Enhancers Active TSS Flanking Active TSS	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	chr16:82910400-82932600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr16:82915800-82953000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr16:82918800-82933400	Weak transcription	NHEK	skin
4	chr16:82922600-82933200	Weak transcription	Fetal Muscle Leg	muscle
5	chr16:82922600-82933200	Weak transcription	Left Ventricle	heart
6	chr16:82925800-82932600	Weak transcription	Right Atrium	heart
7	chr16:82925800-82933000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr16:82926000-82933000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr16:82926000-82933200	Weak transcription	Aorta	Aorta
10	chr16:82926000-82933200	Weak transcription	HMEC	breast
11	chr16:82926200-82930200	Weak transcription	NH-A	brain
12	chr16:82926800-82961200	Weak transcription	HSMM	muscle
13	chr16:82927400-82933000	Weak transcription	HSMMtube	muscle

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