Variant report

Variant	rs4427190
Chromosome Location	chr8:19321385-19321386
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10888163	0.93[ASN][1000 genomes]
rs11204045	0.88[JPT][hapmap]
rs11786904	0.81[ASN][1000 genomes]
rs12155539	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12680768	0.99[ASN][1000 genomes]
rs12682196	0.90[CHB][hapmap]
rs13250181	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs13261732	1.00[CHB][hapmap]
rs13261824	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.87[TSI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13267801	0.81[ASN][1000 genomes]
rs13275706	0.81[ASN][1000 genomes]
rs3185	0.90[CHB][hapmap];0.81[ASN][1000 genomes]
rs34221121	0.97[ASN][1000 genomes]
rs35736969	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4072131	0.88[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs4292704	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs4379462	1.00[CHB][hapmap];0.88[CHD][hapmap];0.82[ASN][1000 genomes]
rs4391455	0.88[ASN][1000 genomes]
rs4409408	1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs4442162	0.88[ASN][1000 genomes]
rs4486225	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4625053	0.93[ASN][1000 genomes]
rs4922030	0.88[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs4922035	0.81[ASN][1000 genomes]
rs4922036	0.84[CEU][hapmap];1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs58551730	0.93[ASN][1000 genomes]
rs62496184	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6586834	0.87[ASN][1000 genomes]
rs6984449	0.81[CEU][hapmap];0.90[CHB][hapmap];0.81[ASN][1000 genomes]
rs6986388	0.81[ASN][1000 genomes]
rs7002357	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs7006155	0.81[ASN][1000 genomes]
rs7011587	0.92[ASN][1000 genomes]
rs7828025	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7836239	0.87[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	nsv1015395	chr8:18489538-19370258	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	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
3	nsv949745	chr8:18826830-19363963	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv1016482	chr8:18834807-19339487	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer 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
5	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
6	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
7	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
8	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
9	esv3693374	chr8:19241970-19359184	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
10	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
11	nsv1022344	chr8:19270143-19324083	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv890623	chr8:19307051-19383697	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	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

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19306800-19322400	Enhancers	Primary T helper cells fromperipheralblood	blood
2	chr8:19310600-19359600	Weak transcription	Ovary	ovary
3	chr8:19313400-19327200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:19314800-19322400	Enhancers	Fetal Thymus	thymus
5	chr8:19315800-19321400	Weak transcription	Adipose Nuclei	Adipose
6	chr8:19316200-19339200	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr8:19316400-19322200	Enhancers	Primary T cells fromperipheralblood	blood
8	chr8:19316400-19323800	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr8:19317600-19321800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr8:19317600-19325800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr8:19318000-19321400	Weak transcription	Fetal Brain Female	brain
12	chr8:19318000-19323200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr8:19318200-19322000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr8:19318200-19323400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr8:19318200-19325600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr8:19318400-19322000	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr8:19318400-19323200	Enhancers	Primary T cells from cord blood	blood
18	chr8:19318600-19322800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr8:19318600-19322800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr8:19318600-19325800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:19318800-19323400	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr8:19318800-19326600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr8:19318800-19332600	Weak transcription	Primary B cells from peripheral blood	blood
24	chr8:19319000-19322000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr8:19319400-19323400	Strong transcription	Primary B cells from cord blood	blood
26	chr8:19319400-19326600	Weak transcription	Right Ventricle	heart
27	chr8:19319400-19327800	Weak transcription	Right Atrium	heart
28	chr8:19319400-19329000	Weak transcription	Placenta	Placenta
29	chr8:19319600-19325800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr8:19319600-19325800	Weak transcription	Lung	lung
31	chr8:19319600-19326000	Weak transcription	Gastric	stomach
32	chr8:19319600-19326200	Weak transcription	Left Ventricle	heart
33	chr8:19319600-19327800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr8:19319600-19362800	Weak transcription	Spleen	Spleen
35	chr8:19319800-19322000	Weak transcription	A549	lung
36	chr8:19319800-19332200	Weak transcription	Pancreas	Pancrea
37	chr8:19320200-19321800	Enhancers	HepG2	liver
38	chr8:19320200-19327800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr8:19320200-19329200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr8:19320800-19321400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr8:19320800-19321600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr8:19321200-19321800	Enhancers	Fetal Brain Male	brain
43	chr8:19321200-19322000	Enhancers	Thymus	Thymus
44	chr8:19321200-19322400	Enhancers	Primary T killer memory cells from peripheral blood	blood

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