Variant report

Variant	rs10834194
Chromosome Location	chr11:23810971-23810972
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10430919	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10500969	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10732217	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10732218	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10742002	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10742003	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10742004	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10767117	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10767121	0.82[ASN][1000 genomes]
rs10767123	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10834191	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10834193	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10834196	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10834197	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10834198	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10834199	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12419586	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1528552	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1528553	0.88[AMR][1000 genomes]
rs3886450	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4131590	0.80[ASN][1000 genomes]
rs4131591	0.81[ASN][1000 genomes]
rs4315068	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4316509	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7113510	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7118415	0.82[ASN][1000 genomes]
rs7948427	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7951414	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7951424	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7951537	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7951542	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7951878	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv553757	chr11:23564329-23896729	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv897062	chr11:23687928-24031627	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916840	chr11:23710275-24064119	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv897063	chr11:23723766-23940407	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv897064	chr11:23767292-23859991	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv897065	chr11:23767292-23882931	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv897066	chr11:23777459-23859991	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv897067	chr11:23777459-23861558	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv897068	chr11:23777459-23882931	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv553765	chr11:23781534-23833286	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv553766	chr11:23781534-23841175	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv467741	chr11:23781534-23944659	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv553767	chr11:23781534-23944659	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv467742	chr11:23783338-23841175	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv467743	chr11:23783338-23841175	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv553768	chr11:23783338-23841175	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
17	nsv1054145	chr11:23796462-23860421	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
18	nsv1053104	chr11:23796462-23870291	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
19	nsv1054249	chr11:23796462-23883614	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
20	nsv469943	chr11:23796710-23859991	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
21	nsv527858	chr11:23796711-23859991	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
22	nsv553769	chr11:23796711-23864290	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
23	nsv897069	chr11:23801412-23864290	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
24	nsv553770	chr11:23801412-23865129	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:23801200-23811000	Weak transcription	HSMM	muscle
2	chr11:23806200-23811200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:23810400-23812200	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr11:23810600-23811200	Enhancers	Colonic Mucosa	Colon
5	chr11:23810600-23811400	Enhancers	Rectal Mucosa Donor 29	rectum
6	chr11:23810600-23811800	Enhancers	Pancreas	Pancrea
7	chr11:23810600-23811800	Enhancers	Dnd41	blood
8	chr11:23810600-23811800	Enhancers	HepG2	liver
9	chr11:23810600-23812000	Enhancers	Stomach Mucosa	stomach
10	chr11:23810600-23812200	Enhancers	Fetal Intestine Large	intestine
11	chr11:23810600-23812200	Enhancers	Fetal Intestine Small	intestine
12	chr11:23810600-23812200	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr11:23810800-23811200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr11:23810800-23811400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr11:23810800-23811800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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