Variant report

Variant	rs2293272
Chromosome Location	chr2:48787733-48787734
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 84 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10495953	1.00[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11125176	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11676150	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11678306	0.91[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11680574	0.91[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs11681276	0.91[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11681426	0.87[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11681868	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11683611	0.86[EUR][1000 genomes]
rs11693429	0.91[CEU][hapmap];0.81[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11693559	0.91[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11693691	0.91[CEU][hapmap];0.81[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12475789	0.80[ASN][1000 genomes]
rs12990079	0.89[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12992755	1.00[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12992870	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12999304	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13010692	0.88[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13011288	0.85[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs13014112	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13016899	0.81[ASN][1000 genomes]
rs13025488	0.91[CEU][hapmap];0.85[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13027618	0.87[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13030948	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13031184	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13034063	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13034951	0.87[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17037412	0.80[CHB][hapmap]
rs17039250	0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1996970	0.86[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs2103112	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2177489	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2293270	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2293271	1.00[ASN][1000 genomes]
rs2293274	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2349098	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2882084	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3749142	0.85[CHB][hapmap];0.90[JPT][hapmap];0.96[YRI][hapmap];0.82[ASN][1000 genomes]
rs3749144	0.91[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3749145	0.91[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3792234	1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.90[ASN][1000 genomes]
rs3792235	0.91[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap];0.92[YRI][hapmap];0.82[ASN][1000 genomes]
rs3792236	0.90[CEU][hapmap];0.85[CHB][hapmap];0.89[JPT][hapmap];0.91[YRI][hapmap];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3792237	0.91[CEU][hapmap];0.81[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3792238	0.86[JPT][hapmap]
rs3828340	1.00[CEU][hapmap];0.80[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4566410	0.91[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4953593	0.91[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs55641971	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55700200	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs55858189	0.89[EUR][1000 genomes]
rs56111874	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62135201	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62135231	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62135232	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62135233	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62135236	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6545048	0.91[ASN][1000 genomes]
rs66888174	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6709043	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6710565	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs6712592	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6712724	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6716291	0.85[CHB][hapmap];0.90[JPT][hapmap];0.92[YRI][hapmap];0.80[ASN][1000 genomes]
rs6722556	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6727929	1.00[CEU][hapmap];0.85[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6729860	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6732365	1.00[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap];0.85[YRI][hapmap];0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6737732	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6741341	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6741677	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6742725	0.83[EUR][1000 genomes]
rs6757847	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6761796	0.82[ASN][1000 genomes]
rs940389	0.91[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];0.96[YRI][hapmap];0.82[ASN][1000 genomes]

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	nsv1005954	chr2:48692696-48905723	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats 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
2	nsv535682	chr2:48692696-48905723	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv833981	chr2:48705444-48878179	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1007491	chr2:48752185-48796441	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv535683	chr2:48752185-48796441	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv581776	chr2:48763382-48913019	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1000419	chr2:48766957-48795327	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1010494	chr2:48767055-49027310	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
9	nsv1002793	chr2:48771220-49466550	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2293272	STON1-GTF2A1L	cis	lung	GTEx
rs2293272	STON1	cis	Esophagus Muscularis	GTEx

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48759000-48827600	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr2:48759200-48793200	Weak transcription	Fetal Lung	lung
3	chr2:48767200-48807800	Weak transcription	Aorta	Aorta
4	chr2:48768000-48793800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr2:48772600-48788000	Weak transcription	Lung	lung
6	chr2:48773000-48808800	Weak transcription	Right Ventricle	heart
7	chr2:48775800-48793600	Weak transcription	Placenta	Placenta
8	chr2:48776600-48794000	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr2:48777200-48807800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr2:48779200-48789800	Weak transcription	Ovary	ovary
11	chr2:48779400-48800200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr2:48780600-48793800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr2:48781200-48793000	Weak transcription	Colon Smooth Muscle	Colon
14	chr2:48781200-48793800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr2:48781400-48789800	Weak transcription	Fetal Stomach	stomach
16	chr2:48781800-48789400	Weak transcription	Stomach Smooth Muscle	stomach
17	chr2:48785400-48788200	Enhancers	Fetal Muscle Leg	muscle
18	chr2:48786000-48788400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr2:48786000-48793600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr2:48786000-48793600	Weak transcription	Fetal Kidney	kidney
21	chr2:48786600-48788400	Enhancers	Brain Cingulate Gyrus	brain
22	chr2:48786800-48788200	Enhancers	Brain Germinal Matrix	brain
23	chr2:48786800-48788400	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr2:48786800-48788400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:48786800-48788400	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr2:48787000-48788400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:48787000-48788400	Enhancers	Brain Anterior Caudate	brain
28	chr2:48787000-48788600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr2:48787000-48790000	Weak transcription	Spleen	Spleen
30	chr2:48787200-48788400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr2:48787200-48788600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr2:48787200-48788600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr2:48787200-48788600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr2:48787200-48788600	Enhancers	Brain Hippocampus Middle	brain
35	chr2:48787400-48788000	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr2:48787400-48788000	Enhancers	Brain Angular Gyrus	brain
37	chr2:48787400-48788200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr2:48787400-48788200	Enhancers	Fetal Muscle Trunk	muscle
39	chr2:48787400-48788400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr2:48787400-48788400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr2:48787400-48788400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr2:48787400-48788600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr2:48787400-48788600	Enhancers	H1 Cell Line	embryonic stem cell
44	chr2:48787600-48787800	Enhancers	Esophagus	oesophagus
45	chr2:48787600-48788000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr2:48787600-48788200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr2:48787600-48788200	Enhancers	Placenta Amnion	Placenta Amnion
48	chr2:48787600-48788200	Enhancers	Right Atrium	heart
49	chr2:48787600-48788200	Enhancers	GM12878-XiMat	blood
50	chr2:48787600-48788400	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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