Variant report

Variant	rs10743369
Chromosome Location	chr12:20531157-20531158
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10734701	1.00[ASN][1000 genomes]
rs10743370	0.92[CEU][hapmap];0.83[YRI][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10770655	1.00[ASN][1000 genomes]
rs10841501	0.87[CEU][hapmap];0.89[LWK][hapmap];0.84[MEX][hapmap];0.90[TSI][hapmap];0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10841515	1.00[ASN][1000 genomes]
rs12370696	1.00[ASN][1000 genomes]
rs1373572	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1373573	0.95[CEU][hapmap];0.87[LWK][hapmap];0.84[MEX][hapmap];0.80[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1444631	1.00[ASN][1000 genomes]
rs1444633	1.00[ASN][1000 genomes]
rs1530445	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1822751	1.00[ASN][1000 genomes]
rs1822752	0.87[CEU][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1822753	1.00[ASN][1000 genomes]
rs1822756	0.95[CEU][hapmap];0.88[YRI][hapmap];0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2417850	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3919734	0.89[YRI][hapmap];0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4762752	1.00[ASN][1000 genomes]
rs4762951	1.00[ASN][1000 genomes]
rs5007546	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs5014038	1.00[ASN][1000 genomes]
rs7133921	1.00[ASN][1000 genomes]
rs7299430	1.00[ASN][1000 genomes]
rs7305462	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7964191	1.00[ASN][1000 genomes]
rs7964703	1.00[ASN][1000 genomes]
rs7979838	1.00[ASN][1000 genomes]
rs935258	0.91[CEU][hapmap];0.89[YRI][hapmap];0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20525600-20531400	Weak transcription	Osteobl	bone
2	chr12:20525600-20543000	Weak transcription	NHDF-Ad	bronchial
3	chr12:20526400-20531600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:20526400-20537600	Weak transcription	Fetal Stomach	stomach
5	chr12:20526600-20536800	Enhancers	Colon Smooth Muscle	Colon
6	chr12:20526800-20541000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr12:20528000-20531400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr12:20528000-20532000	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr12:20528000-20536600	Weak transcription	Left Ventricle	heart
10	chr12:20528600-20532000	Weak transcription	Aorta	Aorta
11	chr12:20528600-20542000	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr12:20528800-20532400	Weak transcription	Right Atrium	heart
13	chr12:20529200-20532600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr12:20530000-20532200	Weak transcription	Fetal Intestine Small	intestine
15	chr12:20530000-20534600	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr12:20530200-20532200	Enhancers	Hela-S3	cervix
17	chr12:20530600-20531400	Enhancers	Fetal Heart	heart
18	chr12:20530800-20532400	Enhancers	HUVEC	blood vessel
19	chr12:20531000-20531600	Enhancers	Fetal Intestine Large	intestine
20	chr12:20531000-20532200	Weak transcription	Stomach Smooth Muscle	stomach
21	chr12:20531000-20532800	Enhancers	A549	lung

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