Variant report

Variant	rs7222759
Chromosome Location	chr17:17526049-17526050
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs11651957	0.91[EUR][1000 genomes]
rs11659047	0.89[EUR][1000 genomes]
rs28454257	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28583584	0.81[EUR][1000 genomes]
rs28652618	0.81[EUR][1000 genomes]
rs28715719	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28884183	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56044345	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56177028	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56327101	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs57638011	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62066215	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62066216	0.83[EUR][1000 genomes]
rs7214988	0.81[EUR][1000 genomes]
rs7217764	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7219568	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7224725	0.81[EUR][1000 genomes]
rs73978990	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8071007	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8074981	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs8076601	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs8077671	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9896285	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9910151	0.96[EUR][1000 genomes]
rs9911823	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9912678	0.81[EUR][1000 genomes]
rs9914118	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9944423	0.81[EUR][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	nsv907748	chr17:17412032-17782404	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
2	nsv1065270	chr17:17430116-17823086	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
3	nsv543236	chr17:17430116-17823086	Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
4	nsv833384	chr17:17491483-17645648	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv869118	chr17:17509896-17599850	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	esv20304	chr17:17525592-17533785	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 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	chr17:17517200-17529400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr17:17524800-17526200	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr17:17525200-17527200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr17:17525400-17527000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr17:17525400-17527000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr17:17525400-17527200	Weak transcription	Spleen	Spleen
7	chr17:17525400-17531800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr17:17525600-17527000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr17:17525600-17527000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr17:17525600-17529400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr17:17525800-17526400	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr17:17525800-17526600	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr17:17525800-17526800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr17:17525800-17527000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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