Variant report

Variant	rs6504635
Chromosome Location	chr17:45057826-45057827
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs11651232	0.88[ASN][1000 genomes]
rs11651386	0.84[ASN][1000 genomes]
rs11656290	0.86[ASN][1000 genomes]
rs11656787	0.90[ASN][1000 genomes]
rs11657300	0.84[ASN][1000 genomes]
rs12449354	0.87[ASN][1000 genomes]
rs12603324	0.85[ASN][1000 genomes]
rs16941434	0.90[ASN][1000 genomes]
rs2316327	0.88[ASN][1000 genomes]
rs2316757	0.90[ASN][1000 genomes]
rs2316759	0.89[ASN][1000 genomes]
rs2317995	0.90[ASN][1000 genomes]
rs2317996	0.90[ASN][1000 genomes]
rs2873608	0.90[ASN][1000 genomes]
rs3851794	0.90[ASN][1000 genomes]
rs3851797	0.90[ASN][1000 genomes]
rs3851800	0.90[ASN][1000 genomes]
rs3851802	0.90[ASN][1000 genomes]
rs3863499	0.86[ASN][1000 genomes]
rs3892426	0.90[ASN][1000 genomes]
rs3892427	0.89[ASN][1000 genomes]
rs3892428	0.90[ASN][1000 genomes]
rs3892678	0.90[ASN][1000 genomes]
rs3901590	0.90[ASN][1000 genomes]
rs4274483	0.90[ASN][1000 genomes]
rs4305136	0.90[ASN][1000 genomes]
rs4468691	0.90[ASN][1000 genomes]
rs4569351	0.90[ASN][1000 genomes]
rs4968294	0.88[ASN][1000 genomes]
rs4968295	0.89[ASN][1000 genomes]
rs4968296	0.89[ASN][1000 genomes]
rs61173406	0.86[ASN][1000 genomes]
rs62075930	0.90[ASN][1000 genomes]
rs6504637	0.90[ASN][1000 genomes]
rs6504638	0.90[ASN][1000 genomes]
rs6504640	0.90[ASN][1000 genomes]
rs6504647	0.90[ASN][1000 genomes]
rs7210126	0.90[ASN][1000 genomes]
rs7214665	0.90[ASN][1000 genomes]
rs7219480	0.90[ASN][1000 genomes]
rs7221913	0.90[ASN][1000 genomes]
rs8064764	0.90[ASN][1000 genomes]
rs8064863	0.89[ASN][1000 genomes]
rs8065072	0.90[ASN][1000 genomes]
rs8065103	0.90[ASN][1000 genomes]
rs8067295	0.96[EUR][1000 genomes]
rs8068375	0.90[ASN][1000 genomes]
rs8069682	0.90[ASN][1000 genomes]
rs8071977	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8073175	0.90[ASN][1000 genomes]
rs8073261	0.90[ASN][1000 genomes]
rs8074704	0.90[ASN][1000 genomes]
rs8074861	0.90[ASN][1000 genomes]
rs8075457	0.88[ASN][1000 genomes]
rs8078196	0.90[ASN][1000 genomes]
rs8078665	0.90[ASN][1000 genomes]
rs8081157	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9891441	0.90[ASN][1000 genomes]
rs9891658	0.85[ASN][1000 genomes]
rs9910512	0.90[ASN][1000 genomes]
rs9989485	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3492820	chr17:44174959-45161556	Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv3492821	chr17:44174959-45161556	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	esv3502492	chr17:44305975-45169159	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	esv3502493	chr17:44305975-45169159	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
5	nsv531823	chr17:44485771-45067769	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
6	nsv908562	chr17:44828931-45102413	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
7	nsv949295	chr17:44836653-45080757	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
8	nsv833466	chr17:45020360-45204537	Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
9	nsv1062983	chr17:45030095-45789543	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6504635	RPRML	cis	Muscle Skeletal	GTEx

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45056800-45069000	Weak transcription	Gastric	stomach
2	chr17:45057000-45058400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr17:45057000-45059600	Weak transcription	HepG2	liver
4	chr17:45057000-45061200	Weak transcription	Pancreas	Pancrea
5	chr17:45057000-45065600	Weak transcription	Brain Substantia Nigra	brain
6	chr17:45057000-45078400	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr17:45057200-45058400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr17:45057200-45086800	Weak transcription	Right Atrium	heart
9	chr17:45057200-45100000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr17:45057400-45058000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
11	chr17:45057400-45058400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr17:45057400-45058400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr17:45057800-45058000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr17:45057800-45058200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr17:45057800-45082400	Weak transcription	Brain Angular Gyrus	brain

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