Variant report

Variant	rs2265880
Chromosome Location	chr10:54764420-54764421
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:54764008..54766836-chr10:54772750..54774326,2	K562	blood:

Extended variants
information (count: 64 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10508984	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10740531	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10824852	0.80[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10824854	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10824856	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10824857	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10824859	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes]
rs10824860	0.86[EUR][1000 genomes]
rs11003335	0.93[EUR][1000 genomes]
rs11003336	0.93[EUR][1000 genomes]
rs11003339	0.89[EUR][1000 genomes]
rs11003340	0.88[EUR][1000 genomes]
rs11003341	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes]
rs11003343	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes]
rs11812875	0.94[EUR][1000 genomes]
rs11819148	0.94[EUR][1000 genomes]
rs12360114	0.88[EUR][1000 genomes]
rs1343046	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1343047	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1343048	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1418915	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1418916	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1539513	0.80[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1573147	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1917190	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes]
rs1917194	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1917195	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1917196	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1917197	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1917205	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1935921	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1935922	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1949813	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1949814	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1984275	0.85[ASN][1000 genomes]
rs2066435	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2066437	0.82[ASN][1000 genomes]
rs2066438	0.83[ASN][1000 genomes]
rs2177608	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2248319	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2248678	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2253152	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2253266	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2264663	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2462479	1.00[CEU][hapmap];0.95[JPT][hapmap];0.89[EUR][1000 genomes]
rs2488605	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2492354	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2891425	0.90[CHB][hapmap];0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2891426	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7069155	0.94[EUR][1000 genomes]
rs7085307	0.81[EUR][1000 genomes]
rs7092980	0.80[CEU][hapmap];0.89[CHB][hapmap];0.89[JPT][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7097052	0.81[EUR][1000 genomes]
rs72800376	0.88[EUR][1000 genomes]
rs72800377	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895404	chr10:54545590-54850707	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv831877	chr10:54565135-54764638	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1043809	chr10:54645158-54860817	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv540627	chr10:54645158-54860817	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv467201	chr10:54697623-54929003	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv550906	chr10:54697623-54929003	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv470939	chr10:54700783-54917339	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv467202	chr10:54735164-54830687	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv550907	chr10:54735164-54830687	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2265880	RP11-319F12.2	cis	Thyroid	GTEx

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54734600-54764600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:54757200-54766400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr10:54759800-54767200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr10:54760200-54765800	Weak transcription	Stomach Mucosa	stomach
5	chr10:54760800-54764800	Weak transcription	Liver	Liver
6	chr10:54760800-54765600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr10:54761000-54764800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr10:54761000-54766000	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr10:54763200-54765000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr10:54763400-54765400	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr10:54763400-54765800	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr10:54764400-54764600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr10:54764400-54764600	Enhancers	Fetal Intestine Small	intestine
14	chr10:54764400-54764600	Enhancers	Fetal Kidney	kidney
15	chr10:54764400-54771200	Enhancers	HepG2	liver

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