Variant report

Variant	rs13270069
Chromosome Location	chr8:11579171-11579172
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11538562..11541468-chr8:11578782..11581146,2	K562	blood:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11250160	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs13267318	0.91[CEU][hapmap];0.91[CHB][hapmap];0.93[JPT][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2409807	0.90[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs4410868	1.00[CEU][hapmap];0.90[CHB][hapmap];0.92[JPT][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6601604	1.00[CEU][hapmap];0.81[CHB][hapmap];0.92[JPT][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6983129	1.00[CHB][hapmap];0.84[JPT][hapmap]

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	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1017865	chr8:11377795-11579954	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv917963	chr8:11540723-11751798	Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv1027378	chr8:11541739-11858466	Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv1028229	chr8:11575762-11805961	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv539475	chr8:11575762-11805961	Flanking Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11575200-11581800	Enhancers	Fetal Heart	heart
2	chr8:11576200-11584800	Enhancers	Liver	Liver
3	chr8:11577200-11579200	Enhancers	Left Ventricle	heart
4	chr8:11577200-11579400	Enhancers	Right Ventricle	heart
5	chr8:11577400-11579200	Flanking Active TSS	Ovary	ovary
6	chr8:11577600-11579200	Bivalent Enhancer	Placenta	Placenta
7	chr8:11577600-11579800	Genic enhancers	Fetal Intestine Small	intestine
8	chr8:11577600-11582600	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr8:11577800-11579800	Weak transcription	Stomach Mucosa	stomach
10	chr8:11578200-11579200	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr8:11578400-11579200	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:11578600-11579200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
13	chr8:11578600-11579200	Genic enhancers	Right Atrium	heart
14	chr8:11578600-11579200	Enhancers	Spleen	Spleen
15	chr8:11578800-11579200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
16	chr8:11578800-11579200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
17	chr8:11578800-11579200	Enhancers	Pancreas	Pancrea
18	chr8:11578800-11579400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
19	chr8:11578800-11579400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr8:11578800-11581400	Weak transcription	Duodenum Mucosa	Duodenum
21	chr8:11578800-11581800	Weak transcription	HepG2	liver
22	chr8:11579000-11579200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
23	chr8:11579000-11579200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
24	chr8:11579000-11579200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
25	chr8:11579000-11579200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr8:11579000-11579200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
27	chr8:11579000-11579400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr8:11579000-11579400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
29	chr8:11579000-11580000	Weak transcription	Gastric	stomach

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