Variant report

Variant	rs512495
Chromosome Location	chr11:59876036-59876037
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs107903	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10897009	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11230147	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11230153	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11230155	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1125357	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11600716	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12226022	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1303615	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1303621	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1441586	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17528859	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17529983	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1786137	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1813217	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2070970	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2165525	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2583471	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2583476	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2847655	0.82[EUR][1000 genomes]
rs2847663	0.85[EUR][1000 genomes]
rs2847664	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2847666	0.81[EUR][1000 genomes]
rs2847667	0.81[EUR][1000 genomes]
rs2847668	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2855017	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs483629	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs487997	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4939311	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4939312	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4939314	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs502419	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs502581	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs504272	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs510518	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs514266	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs516478	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs521952	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs525794	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs534273	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs540170	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs555635	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs556917	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55847558	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs563803	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs564912	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs569046	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs574695	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs574704	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs574798	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs580064	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs580817	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs581133	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs583791	0.81[EUR][1000 genomes]
rs602396	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs610932	0.85[EUR][1000 genomes]
rs61901691	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs624663	0.81[EUR][1000 genomes]
rs631853	0.82[EUR][1000 genomes]
rs632185	0.81[EUR][1000 genomes]
rs634475	0.82[EUR][1000 genomes]
rs652354	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs662196	0.82[EUR][1000 genomes]
rs7124974	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs920573	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs983392	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832173	chr11:59788884-59940560	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv468579	chr11:59814287-59975400	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv555150	chr11:59814287-59975400	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59869800-59876800	Weak transcription	Small Intestine	intestine
2	chr11:59875000-59877400	Enhancers	Fetal Intestine Small	intestine
3	chr11:59875200-59877000	Enhancers	Stomach Mucosa	stomach
4	chr11:59875200-59877200	Enhancers	K562	blood
5	chr11:59875600-59877200	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr11:59875800-59876200	Flanking Active TSS	Duodenum Mucosa	Duodenum
7	chr11:59875800-59877000	Enhancers	Fetal Intestine Large	intestine
8	chr11:59875800-59877000	Enhancers	Rectal Mucosa Donor 29	rectum
9	chr11:59876000-59877000	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr11:59876000-59878800	Weak transcription	Ovary	ovary

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