Variant report

Variant	rs1179500
Chromosome Location	chr2:36724282-36724283
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11692416	0.91[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs11886869	0.87[EUR][1000 genomes]
rs11888819	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs11890094	0.95[CEU][hapmap];0.90[EUR][1000 genomes]
rs11893748	0.95[CEU][hapmap];0.86[EUR][1000 genomes]
rs1403857	0.95[CEU][hapmap];0.87[EUR][1000 genomes]
rs1403858	0.95[CEU][hapmap];0.87[EUR][1000 genomes]
rs1403859	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs17018901	0.95[CEU][hapmap];0.86[EUR][1000 genomes]
rs2021870	0.95[CEU][hapmap];0.88[EUR][1000 genomes]
rs2022210	0.95[CEU][hapmap];0.82[EUR][1000 genomes]
rs3770839	0.86[CEU][hapmap];0.80[EUR][1000 genomes]
rs3770844	0.95[CEU][hapmap];0.87[EUR][1000 genomes]
rs3770845	0.91[CEU][hapmap];0.85[EUR][1000 genomes]
rs3899034	0.91[CEU][hapmap];0.80[EUR][1000 genomes]
rs4670562	0.92[EUR][1000 genomes]
rs60970158	0.93[EUR][1000 genomes]
rs711248	0.97[ASN][1000 genomes]
rs711249	0.91[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7571231	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs7571475	0.86[CEU][hapmap]
rs848530	0.91[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs848533	0.83[CEU][hapmap];0.91[CHB][hapmap];0.85[JPT][hapmap];0.89[ASN][1000 genomes]
rs848537	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs848538	0.87[CEU][hapmap];0.91[CHB][hapmap];0.85[JPT][hapmap];0.89[ASN][1000 genomes]
rs848541	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs950420	0.95[CEU][hapmap];0.92[EUR][1000 genomes]
rs955601	0.89[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833803	chr2:36589065-36745779	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1010985	chr2:36707157-36942066	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv535642	chr2:36707157-36942066	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36688600-36725600	Weak transcription	Small Intestine	intestine
2	chr2:36704800-36736200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:36705000-36743200	Weak transcription	Brain Germinal Matrix	brain
4	chr2:36707000-36740600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:36708600-36739000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:36708800-36726000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr2:36709200-36726800	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr2:36709200-36727200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr2:36709200-36739000	Weak transcription	Colonic Mucosa	Colon
10	chr2:36709400-36726600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr2:36709400-36726800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:36709400-36726800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr2:36710000-36743400	Weak transcription	Primary T cells from cord blood	blood
14	chr2:36710400-36726600	Weak transcription	Duodenum Mucosa	Duodenum
15	chr2:36711200-36726600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr2:36711400-36726400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:36711400-36726400	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr2:36711400-36726600	Weak transcription	Esophagus	oesophagus
19	chr2:36711400-36739200	Weak transcription	Primary B cells from cord blood	blood
20	chr2:36711600-36726800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr2:36711800-36726400	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr2:36712000-36726400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr2:36712000-36726400	Weak transcription	Spleen	Spleen
24	chr2:36712000-36726600	Weak transcription	Fetal Muscle Trunk	muscle
25	chr2:36712000-36726600	Weak transcription	Gastric	stomach
26	chr2:36712600-36726400	Weak transcription	Primary hematopoietic stem cells	blood
27	chr2:36712600-36727000	Weak transcription	Right Ventricle	heart
28	chr2:36712800-36726400	Weak transcription	Fetal Brain Female	brain
29	chr2:36712800-36726800	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr2:36713000-36726400	Weak transcription	Left Ventricle	heart
31	chr2:36713000-36733200	Weak transcription	Pancreas	Pancrea
32	chr2:36713600-36726600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr2:36713600-36739200	Weak transcription	Fetal Muscle Leg	muscle
34	chr2:36713800-36726600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr2:36713800-36726600	Weak transcription	Ovary	ovary
36	chr2:36713800-36733200	Weak transcription	Stomach Mucosa	stomach
37	chr2:36713800-36789600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr2:36714400-36725400	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr2:36714400-36726600	Weak transcription	Fetal Stomach	stomach
40	chr2:36714600-36725400	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr2:36714800-36726000	Weak transcription	Fetal Lung	lung
42	chr2:36715400-36726400	Weak transcription	Adipose Nuclei	Adipose
43	chr2:36716200-36726600	Weak transcription	Fetal Intestine Small	intestine
44	chr2:36717000-36724400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr2:36717200-36725600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr2:36717200-36733000	Genic enhancers	A549	lung
47	chr2:36717400-36726600	Weak transcription	Brain Cingulate Gyrus	brain
48	chr2:36717400-36744400	Weak transcription	Brain Angular Gyrus	brain
49	chr2:36717600-36727000	Strong transcription	HepG2	liver
50	chr2:36718000-36726600	Weak transcription	Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links