Variant report

Variant	rs11045203
Chromosome Location	chr12:20540124-20540125
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10505865	0.83[ASN][1000 genomes]
rs10732533	0.82[ASN][1000 genomes]
rs10732534	0.82[ASN][1000 genomes]
rs10743372	0.82[ASN][1000 genomes]
rs10743373	0.82[ASN][1000 genomes]
rs10743374	0.82[ASN][1000 genomes]
rs10770649	0.90[ASN][1000 genomes]
rs10770650	0.93[ASN][1000 genomes]
rs10770651	0.83[ASN][1000 genomes]
rs10770652	0.92[ASN][1000 genomes]
rs10770653	0.82[ASN][1000 genomes]
rs10770656	0.88[ASN][1000 genomes]
rs10841509	0.89[ASN][1000 genomes]
rs10841510	0.92[ASN][1000 genomes]
rs10841512	0.83[ASN][1000 genomes]
rs10841513	0.92[ASN][1000 genomes]
rs10841516	0.92[ASN][1000 genomes]
rs11045206	0.92[ASN][1000 genomes]
rs11045207	0.92[ASN][1000 genomes]
rs11045211	0.93[ASN][1000 genomes]
rs11045218	0.92[ASN][1000 genomes]
rs11045220	0.92[ASN][1000 genomes]
rs11045221	0.92[ASN][1000 genomes]
rs11045222	0.90[ASN][1000 genomes]
rs11045223	0.93[ASN][1000 genomes]
rs11045224	0.83[ASN][1000 genomes]
rs11045225	0.83[ASN][1000 genomes]
rs11045226	0.83[ASN][1000 genomes]
rs11045227	0.82[ASN][1000 genomes]
rs11045228	0.82[ASN][1000 genomes]
rs11045230	0.92[ASN][1000 genomes]
rs12297116	0.93[ASN][1000 genomes]
rs12370745	0.82[ASN][1000 genomes]
rs1348583	0.82[ASN][1000 genomes]
rs1444628	0.83[ASN][1000 genomes]
rs1444629	0.83[ASN][1000 genomes]
rs1444630	0.83[ASN][1000 genomes]
rs1444634	0.83[ASN][1000 genomes]
rs1444635	0.83[ASN][1000 genomes]
rs1444641	0.82[ASN][1000 genomes]
rs1444643	0.83[ASN][1000 genomes]
rs1444644	0.83[ASN][1000 genomes]
rs1444645	0.83[ASN][1000 genomes]
rs1444646	0.82[ASN][1000 genomes]
rs16922851	0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1838447	0.83[ASN][1000 genomes]
rs1838448	0.82[ASN][1000 genomes]
rs4762955	0.83[ASN][1000 genomes]
rs5014033	0.82[ASN][1000 genomes]
rs5014034	0.82[ASN][1000 genomes]
rs5014035	0.82[ASN][1000 genomes]
rs5014036	0.82[ASN][1000 genomes]
rs5014037	0.82[ASN][1000 genomes]
rs5014039	0.82[ASN][1000 genomes]
rs5014040	0.82[ASN][1000 genomes]
rs60593141	0.94[ASN][1000 genomes]
rs60977432	0.92[ASN][1000 genomes]
rs6487083	0.82[ASN][1000 genomes]
rs6487084	0.82[ASN][1000 genomes]
rs6487085	0.82[ASN][1000 genomes]
rs6487086	0.82[ASN][1000 genomes]
rs7136586	0.93[ASN][1000 genomes]
rs71450706	0.83[ASN][1000 genomes]
rs7310385	0.83[ASN][1000 genomes]
rs7314448	0.82[ASN][1000 genomes]
rs73232485	0.93[ASN][1000 genomes]
rs7954501	0.83[ASN][1000 genomes]
rs7957567	0.83[ASN][1000 genomes]
rs7967538	0.83[ASN][1000 genomes]
rs978349	0.83[ASN][1000 genomes]
rs9805045	0.82[ASN][1000 genomes]

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	nsv1048067	chr12:20363755-20874845	Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv541408	chr12:20363755-20874845	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1046870	chr12:20509914-20711535	Active TSS Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
4	nsv541409	chr12:20509914-20711535	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
5	nsv1042315	chr12:20531641-20629866	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv3322484	chr12:20537910-20540458	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3446622	chr12:20538035-20540133	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20525600-20543000	Weak transcription	NHDF-Ad	bronchial
2	chr12:20526800-20541000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr12:20528600-20542000	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr12:20533000-20541400	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr12:20533200-20544800	Weak transcription	Right Atrium	heart
6	chr12:20534600-20542200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr12:20536800-20540200	Weak transcription	Colon Smooth Muscle	Colon
8	chr12:20536800-20542000	Weak transcription	Aorta	Aorta
9	chr12:20536800-20542000	Weak transcription	Right Ventricle	heart
10	chr12:20536800-20542200	Weak transcription	Stomach Smooth Muscle	stomach
11	chr12:20536800-20542400	Weak transcription	A549	lung
12	chr12:20537000-20541400	Weak transcription	Hela-S3	cervix
13	chr12:20537800-20542000	Weak transcription	Fetal Intestine Small	intestine
14	chr12:20538200-20550400	Weak transcription	HUVEC	blood vessel
15	chr12:20538200-20558000	Weak transcription	Left Ventricle	heart
16	chr12:20539600-20540200	ZNF genes & repeats	Fetal Intestine Large	intestine
17	chr12:20540000-20540200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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