Variant report

Variant	rs16826737
Chromosome Location	chr2:134357339-134357340
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10803537	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11675147	0.82[CHB][hapmap]
rs12622133	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12623896	0.90[ASN][1000 genomes]
rs13412991	0.82[CHB][hapmap]
rs16826437	0.95[CHB][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];1.00[EUR][1000 genomes]
rs16826512	1.00[ASW][hapmap];0.90[CHB][hapmap];0.83[CHD][hapmap];0.91[GIH][hapmap];0.86[MEX][hapmap];1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs1897433	0.82[CHB][hapmap]
rs60546774	1.00[EUR][1000 genomes]
rs6705688	1.00[ASW][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6706405	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6735323	0.88[ASN][1000 genomes]
rs6748301	0.87[ASN][1000 genomes]
rs876204	0.90[CHB][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997821	chr2:133868822-134360220	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv535927	chr2:133868822-134360220	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1003624	chr2:134126928-134583203	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1006101	chr2:134263288-134973917	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
5	nsv516644	chr2:134301130-134391214	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv431713	chr2:134316522-134413604	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1013713	chr2:134322236-134644574	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv535931	chr2:134322236-134644574	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:134345400-134360000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:134345400-134360000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr2:134352200-134360000	Weak transcription	NHEK	skin
4	chr2:134354000-134359200	Enhancers	Brain Anterior Caudate	brain
5	chr2:134354200-134358800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
6	chr2:134354200-134359200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:134354200-134359200	Enhancers	Brain Cingulate Gyrus	brain
8	chr2:134354400-134359000	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr2:134354600-134357800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr2:134354600-134359200	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr2:134354600-134362600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr2:134354800-134357600	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr2:134355000-134358600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr2:134355000-134359800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr2:134355000-134362200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:134355200-134358800	Enhancers	Brain Angular Gyrus	brain
17	chr2:134355800-134361200	Enhancers	Fetal Muscle Leg	muscle
18	chr2:134356000-134358400	Enhancers	Fetal Heart	heart
19	chr2:134356000-134358800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr2:134356000-134358800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:134356200-134358000	Enhancers	Liver	Liver
22	chr2:134356200-134358600	Enhancers	Left Ventricle	heart
23	chr2:134356200-134359000	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:134356200-134359800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr2:134356400-134357400	Enhancers	Right Atrium	heart
26	chr2:134356400-134358600	Enhancers	Brain Germinal Matrix	brain
27	chr2:134356400-134358800	Enhancers	Fetal Brain Female	brain
28	chr2:134356400-134359000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:134356400-134359200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr2:134356600-134359800	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr2:134356800-134357800	Flanking Active TSS	Brain Hippocampus Middle	brain
32	chr2:134356800-134358800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr2:134356800-134360600	Enhancers	Fetal Brain Male	brain
34	chr2:134357000-134359000	Enhancers	Right Ventricle	heart
35	chr2:134357200-134357400	Flanking Active TSS	Brain Substantia Nigra	brain
36	chr2:134357200-134357400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr2:134357200-134357600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr2:134357200-134358200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr2:134357200-134358400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr2:134357200-134358400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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