Variant report

Variant	rs10811542
Chromosome Location	chr9:21429520-21429521
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10811535	1.00[CEU][hapmap]
rs10811545	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10811549	0.82[EUR][1000 genomes]
rs10811551	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs10964981	1.00[CEU][hapmap]
rs10964982	1.00[CEU][hapmap]
rs10964985	1.00[CEU][hapmap]
rs10964987	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10964989	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10964998	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10965002	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[EUR][1000 genomes]
rs10965005	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[EUR][1000 genomes]
rs10965008	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs10965010	0.87[EUR][1000 genomes]
rs10965019	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10965024	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[EUR][1000 genomes]
rs10965031	0.84[EUR][1000 genomes]
rs10965034	1.00[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs10965036	1.00[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs1125488	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12156640	1.00[CEU][hapmap]
rs12375583	0.88[EUR][1000 genomes]
rs12376959	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1332180	0.82[EUR][1000 genomes]
rs1332188	0.88[EUR][1000 genomes]
rs16938384	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs16938433	0.88[EUR][1000 genomes]
rs16938435	0.80[EUR][1000 genomes]
rs2383190	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55938615	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56106002	0.88[EUR][1000 genomes]
rs56337511	0.88[EUR][1000 genomes]
rs7034161	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs72703410	0.91[EUR][1000 genomes]
rs72703411	0.84[EUR][1000 genomes]
rs72703417	0.88[EUR][1000 genomes]
rs72703418	0.88[EUR][1000 genomes]
rs72703419	0.88[EUR][1000 genomes]
rs72703426	0.88[EUR][1000 genomes]
rs7861480	0.85[CEU][hapmap]

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	nsv892724	chr9:20690244-21517302	Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	153 gene(s)	inside rSNPs	diseases
2	esv2752289	chr9:21361957-21499624	Weak transcription Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv466297	chr9:21391698-21507589	Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv613758	chr9:21391698-21507589	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv892739	chr9:21407250-21470520	Weak transcription Bivalent Enhancer ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21428200-21430200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr9:21428200-21430200	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr9:21428400-21429800	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr9:21428600-21429600	Enhancers	H1 Cell Line	embryonic stem cell
5	chr9:21428600-21429600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr9:21429000-21429800	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr9:21429000-21430000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr9:21429000-21430000	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr9:21429000-21430000	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr9:21429200-21430000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr9:21429200-21430200	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr9:21429400-21430400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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