Variant report

Variant	rs10467382
Chromosome Location	chr13:49934913-49934914
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11148144	1.00[CHB][hapmap]
rs12323239	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7994157	1.00[ASN][1000 genomes]
rs9316440	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9316441	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9316444	0.84[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9316445	1.00[CHB][hapmap]
rs9526544	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs9526545	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9526546	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9526547	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9526548	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9535204	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9535205	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9535206	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9535207	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9535208	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9535214	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9596087	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[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	nsv900069	chr13:49815405-49976393	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1047311	chr13:49895019-50224227	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv430558	chr13:49914393-50059354	Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv430559	chr13:49930369-50059354	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv430560	chr13:49930643-50059354	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv430562	chr13:49930643-50067246	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv430561	chr13:49930643-50089844	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49876200-49935600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr13:49889000-49944600	Weak transcription	Brain Angular Gyrus	brain
3	chr13:49889000-49947600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr13:49889200-49944600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr13:49895800-49935600	Weak transcription	Esophagus	oesophagus
6	chr13:49912600-49948800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr13:49915000-49941400	Weak transcription	Brain Hippocampus Middle	brain
8	chr13:49922200-49937600	Weak transcription	Fetal Brain Male	brain
9	chr13:49922200-49937600	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr13:49922400-49940800	Weak transcription	Lung	lung
11	chr13:49922400-49946600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr13:49922400-49947800	Weak transcription	Right Ventricle	heart
13	chr13:49922800-49951400	Weak transcription	Gastric	stomach
14	chr13:49923000-49935000	Weak transcription	Fetal Muscle Trunk	muscle
15	chr13:49923200-49935000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr13:49923200-49937800	Weak transcription	Primary B cells from cord blood	blood
17	chr13:49923200-49951200	Weak transcription	Pancreas	Pancrea
18	chr13:49926400-49937600	Weak transcription	Brain Substantia Nigra	brain
19	chr13:49926800-49937800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr13:49929000-49936000	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr13:49929400-49950000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr13:49929600-49936400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr13:49929800-49935200	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr13:49929800-49937000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr13:49929800-49937600	Weak transcription	Liver	Liver
26	chr13:49931000-49935400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr13:49932000-49938000	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr13:49932200-49936600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr13:49932200-49941800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr13:49932200-49944600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr13:49932400-49935000	Weak transcription	HSMM	muscle
32	chr13:49932400-49941400	Weak transcription	NHLF	lung
33	chr13:49932800-49935600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr13:49933800-49935200	Weak transcription	Colon Smooth Muscle	Colon
35	chr13:49933800-49935800	Weak transcription	Fetal Muscle Leg	muscle
36	chr13:49933800-49937200	Weak transcription	Primary hematopoietic stem cells	blood
37	chr13:49933800-49937200	Weak transcription	Fetal Brain Female	brain
38	chr13:49933800-49937800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr13:49933800-49941600	Weak transcription	Ovary	ovary
40	chr13:49934000-49936400	Weak transcription	Brain Anterior Caudate	brain
41	chr13:49934000-49937600	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr13:49934000-49937800	Weak transcription	Primary T cells from cord blood	blood
43	chr13:49934000-49937800	Weak transcription	Adipose Nuclei	Adipose
44	chr13:49934200-49938000	Weak transcription	Stomach Smooth Muscle	stomach
45	chr13:49934200-49941400	Weak transcription	Fetal Heart	heart
46	chr13:49934200-49942600	Weak transcription	Rectal Smooth Muscle	rectum
47	chr13:49934200-49957400	Weak transcription	Left Ventricle	heart
48	chr13:49934800-49935000	Enhancers	Aorta	Aorta

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