Variant report

Variant	rs1363925
Chromosome Location	chr5:37728063-37728064
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1019505	0.91[JPT][hapmap]
rs10461983	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10461984	1.00[CEU][hapmap];0.91[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10941361	1.00[CEU][hapmap];0.91[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11749343	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11749345	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12513493	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12517792	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12519774	1.00[CEU][hapmap];0.91[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12521092	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12651803	1.00[CEU][hapmap];0.91[CHB][hapmap];0.87[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12656733	0.91[CHB][hapmap];0.83[JPT][hapmap]
rs13154033	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13159969	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13171010	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13182737	0.95[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap]
rs13185923	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13187416	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1862577	0.96[CEU][hapmap];0.87[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2973053	0.81[AMR][1000 genomes]
rs2973086	1.00[CEU][hapmap];0.95[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2973088	0.82[AMR][1000 genomes]
rs4431371	1.00[CEU][hapmap];0.92[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4869542	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs677084	1.00[YRI][hapmap]
rs6897494	0.91[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs781794	1.00[YRI][hapmap]
rs870100	0.86[CEU][hapmap];0.91[JPT][hapmap];0.85[AMR][1000 genomes]
rs9292665	0.91[CHB][hapmap];0.83[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026554	chr5:37112133-37734859	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
2	nsv537726	chr5:37112133-37734859	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
3	nsv949716	chr5:37179341-37967352	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
4	nsv1023871	chr5:37330018-37804744	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	nsv537729	chr5:37330018-37804744	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
6	nsv432744	chr5:37374124-37743077	ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv597846	chr5:37430215-37813591	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1030250	chr5:37478163-37734859	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv881383	chr5:37485316-37773877	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37685200-37743200	Weak transcription	Gastric	stomach
2	chr5:37697000-37743800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr5:37704400-37735400	Weak transcription	Brain Angular Gyrus	brain
4	chr5:37710200-37735400	Weak transcription	Brain Substantia Nigra	brain
5	chr5:37716400-37734800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr5:37717600-37737600	Weak transcription	Small Intestine	intestine
7	chr5:37717800-37735200	Weak transcription	Brain Hippocampus Middle	brain
8	chr5:37717800-37735200	Weak transcription	Fetal Brain Male	brain
9	chr5:37717800-37735400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr5:37717800-37735600	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr5:37717800-37756200	Weak transcription	Right Ventricle	heart
12	chr5:37718400-37735400	Weak transcription	Brain Anterior Caudate	brain
13	chr5:37718400-37735400	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr5:37718400-37743200	Weak transcription	Aorta	Aorta
15	chr5:37718400-37745400	Weak transcription	Pancreas	Pancrea
16	chr5:37718400-37755800	Weak transcription	Spleen	Spleen
17	chr5:37718800-37735600	Weak transcription	Colon Smooth Muscle	Colon
18	chr5:37718800-37735600	Weak transcription	Fetal Heart	heart
19	chr5:37719400-37743000	Weak transcription	Fetal Intestine Small	intestine
20	chr5:37720800-37730000	Strong transcription	Primary T cells from cord blood	blood
21	chr5:37721200-37728400	Strong transcription	Left Ventricle	heart
22	chr5:37721200-37730200	Strong transcription	Primary B cells from peripheral blood	blood
23	chr5:37721200-37731800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr5:37721200-37737400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:37721400-37764200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr5:37721800-37729400	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr5:37721800-37731000	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr5:37721800-37731200	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr5:37722000-37729000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr5:37722000-37733600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr5:37722200-37732200	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr5:37722400-37743200	Weak transcription	Esophagus	oesophagus
33	chr5:37722800-37731400	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr5:37723000-37737400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr5:37723200-37738200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr5:37723400-37728600	Weak transcription	Fetal Kidney	kidney
37	chr5:37723400-37736000	Weak transcription	K562	blood
38	chr5:37723400-37738200	Weak transcription	A549	lung
39	chr5:37723600-37737400	Weak transcription	HUVEC	blood vessel
40	chr5:37723800-37735400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr5:37724000-37731200	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr5:37724400-37730400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr5:37724600-37738000	Weak transcription	NHEK	skin
44	chr5:37725000-37731400	Strong transcription	Primary monocytes fromperipheralblood	blood
45	chr5:37725000-37738400	Weak transcription	HMEC	breast
46	chr5:37725200-37735600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr5:37725400-37728800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr5:37725600-37729200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr5:37725600-37729200	Weak transcription	HepG2	liver
50	chr5:37725600-37735400	Weak transcription	NHDF-Ad	bronchial

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links