Variant report

Variant	rs55786763
Chromosome Location	chr8:19389575-19389576
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs12114968	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17128573	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28532825	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2958556	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2958586	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2958590	0.83[ASN][1000 genomes]
rs2958592	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2975456	0.84[ASN][1000 genomes]
rs2975467	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2975468	0.86[ASN][1000 genomes]
rs2975469	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2975484	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2975485	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34240343	0.81[ASN][1000 genomes]
rs4418356	0.87[ASN][1000 genomes]
rs4921658	0.85[ASN][1000 genomes]
rs4922056	0.89[ASN][1000 genomes]
rs4922058	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62493890	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6586841	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6992386	0.85[ASN][1000 genomes]
rs6999592	0.81[ASN][1000 genomes]
rs7002464	0.91[EUR][1000 genomes]
rs73212597	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7817732	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429907	chr8:18578720-19398220	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv533109	chr8:18845845-19456780	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv949636	chr8:18957705-19664732	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv948861	chr8:19199688-19609029	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv949304	chr8:19199688-19625912	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	esv34007	chr8:19252602-19482098	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
7	nsv890624	chr8:19319061-19456270	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv610753	chr8:19364883-19439977	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv890625	chr8:19368697-19799641	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
10	nsv1018057	chr8:19370830-19435399	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1016276	chr8:19374998-19435147	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv1024012	chr8:19377703-19409791	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv890626	chr8:19383697-19483259	Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19375600-19390000	Weak transcription	Right Atrium	heart
2	chr8:19379400-19434200	Weak transcription	Placenta	Placenta
3	chr8:19380800-19394600	Weak transcription	Primary B cells from cord blood	blood
4	chr8:19380800-19397200	Weak transcription	Right Ventricle	heart
5	chr8:19385400-19397200	Weak transcription	Left Ventricle	heart
6	chr8:19385800-19394400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr8:19386400-19398200	Weak transcription	Ovary	ovary
8	chr8:19387000-19393200	Weak transcription	Hela-S3	cervix
9	chr8:19387000-19397000	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr8:19388000-19389600	Enhancers	Primary T cells fromperipheralblood	blood
11	chr8:19388000-19389600	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr8:19388000-19390400	Enhancers	Primary T cells from cord blood	blood
13	chr8:19388000-19390400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr8:19388200-19390400	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr8:19388400-19389600	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr8:19388400-19390200	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr8:19389000-19408000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr8:19389200-19389800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr8:19389400-19389600	Enhancers	Thymus	Thymus
20	chr8:19389400-19390400	Enhancers	A549	lung

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