Variant report

Variant	rs11015810
Chromosome Location	chr10:27771134-27771135
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:27769453..27771996-chr10:27788773..27790956,2	K562	blood:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10082387	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10128112	0.87[ASN][1000 genomes]
rs10508724	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs10764695	0.93[ASN][1000 genomes]
rs10764696	0.87[ASN][1000 genomes]
rs10764697	0.87[ASN][1000 genomes]
rs10764699	0.89[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs10829261	0.87[ASN][1000 genomes]
rs11015807	0.99[ASN][1000 genomes]
rs11015812	0.98[ASN][1000 genomes]
rs11015815	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11015816	0.95[ASN][1000 genomes]
rs11015817	0.95[ASN][1000 genomes]
rs11015821	0.85[AFR][1000 genomes]
rs11015822	0.81[AFR][1000 genomes]
rs11015823	0.87[ASN][1000 genomes]
rs11015826	0.89[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11015832	0.84[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs11015833	0.83[ASN][1000 genomes]
rs11015840	0.84[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs11015856	0.82[CHB][hapmap];0.89[JPT][hapmap]
rs11015858	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs12218420	0.95[ASN][1000 genomes]
rs12220463	0.84[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12242702	1.00[AFR][1000 genomes]
rs12263006	0.87[ASN][1000 genomes]
rs12265154	0.81[AFR][1000 genomes]
rs12569737	0.96[ASN][1000 genomes]
rs12571836	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs12571985	0.95[ASN][1000 genomes]
rs12573111	0.89[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs17756134	0.84[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs1886402	0.94[ASN][1000 genomes]
rs2242356	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs4237384	0.87[ASN][1000 genomes]
rs4345873	0.87[ASN][1000 genomes]
rs4514312	0.89[CHB][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs4634991	0.86[ASN][1000 genomes]
rs61226328	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72629756	0.99[ASN][1000 genomes]
rs72629757	0.99[ASN][1000 genomes]
rs72629758	0.95[ASN][1000 genomes]
rs72629759	0.89[ASN][1000 genomes]
rs72629760	0.89[ASN][1000 genomes]
rs73604009	0.96[AFR][1000 genomes]
rs73604010	0.88[AFR][1000 genomes]
rs74127314	1.00[AFR][1000 genomes]
rs74127330	0.81[AFR][1000 genomes]
rs7475332	0.82[ASN][1000 genomes]
rs9971075	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8614	chr10:27504487-27828406	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv550241	chr10:27569521-28025771	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv1045257	chr10:27572440-27926946	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv1053952	chr10:27659365-27915029	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	esv2750890	chr10:27669479-27774501	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27765200-27771800	Weak transcription	Colon Smooth Muscle	Colon
2	chr10:27767000-27771600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr10:27769200-27772600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr10:27769400-27771800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr10:27769400-27771800	Enhancers	NHEK	skin
6	chr10:27769400-27772000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr10:27769400-27772600	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr10:27770200-27771200	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr10:27770200-27775600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr10:27770400-27771400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr10:27770400-27771800	Enhancers	HMEC	breast
12	chr10:27770600-27771400	Enhancers	Primary hematopoietic stem cells	blood
13	chr10:27770600-27771600	Enhancers	Monocytes-CD14+_RO01746	blood

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