Variant report

Variant	rs1708678
Chromosome Location	chr4:89976467-89976468
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1060693	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11097215	0.83[CEU][hapmap];0.89[JPT][hapmap]
rs12647382	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13143981	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1343921	0.83[CHD][hapmap];0.96[GIH][hapmap]
rs1398947	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1458558	0.85[CHD][hapmap];0.89[JPT][hapmap]
rs1513807	1.00[CEU][hapmap];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1513824	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1533291	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];0.97[TSI][hapmap];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1708660	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1708661	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1708674	0.89[JPT][hapmap]
rs1708675	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1708679	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1708680	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1708682	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1708684	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];0.97[TSI][hapmap];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1795721	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1795728	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1795731	0.83[CHD][hapmap];0.89[JPT][hapmap]
rs1795732	0.89[JPT][hapmap]
rs1795733	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.97[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1807870	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1818494	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2037036	0.89[JPT][hapmap];0.80[TSI][hapmap]
rs2037037	0.89[JPT][hapmap]
rs2458545	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2464513	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2670624	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2670625	0.89[JPT][hapmap]
rs2670626	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.97[TSI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2670629	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2670630	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28498689	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2869987	0.83[CEU][hapmap];0.89[JPT][hapmap]
rs59610544	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60535906	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62308652	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6532094	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6844490	0.89[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap]
rs6846926	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7440590	0.83[CEU][hapmap];0.89[JPT][hapmap];0.80[MEX][hapmap];0.85[TSI][hapmap]
rs7691983	0.83[CEU][hapmap];0.89[JPT][hapmap];0.83[MEX][hapmap];0.85[TSI][hapmap]
rs9307062	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs938266	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs938268	0.83[CEU][hapmap];0.89[JPT][hapmap]

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	nsv470051	chr4:89644931-90643144	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1009354	chr4:89725914-89985155	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1007025	chr4:89837734-90098046	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv537176	chr4:89837734-90098046	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv461577	chr4:89904124-89986326	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
6	nsv594807	chr4:89904124-89986326	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv1002448	chr4:89933385-90128133	Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1708678	SPARCL1	cis	parietal	SCAN

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:89944200-89978000	Weak transcription	Pancreas	Pancrea
2	chr4:89973200-89977000	Weak transcription	Psoas Muscle	Psoas
3	chr4:89973400-89976800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr4:89973400-89977800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:89973400-89977800	Weak transcription	Right Ventricle	heart
6	chr4:89973600-89977800	Weak transcription	Placenta	Placenta
7	chr4:89974600-89976600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr4:89975200-89976800	Enhancers	Fetal Heart	heart
9	chr4:89975200-89977200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr4:89975200-89979200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr4:89975400-89976600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr4:89975400-89976600	Enhancers	HUVEC	blood vessel
13	chr4:89975400-89977000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr4:89975400-89977000	Enhancers	Primary hematopoietic stem cells	blood
15	chr4:89975600-89976600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
16	chr4:89975600-89976600	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr4:89975600-89976600	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr4:89975600-89976800	Enhancers	Fetal Intestine Large	intestine
19	chr4:89975600-89977000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr4:89975600-89977000	Weak transcription	Fetal Brain Male	brain
21	chr4:89975600-89977000	Weak transcription	Hela-S3	cervix
22	chr4:89975600-89977800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:89975600-89978400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr4:89975600-89978800	Active TSS	Duodenum Mucosa	Duodenum
25	chr4:89975800-89976600	Enhancers	Muscle Satellite Cultured Cells	--
26	chr4:89975800-89976600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr4:89975800-89976600	Enhancers	Osteobl	bone
28	chr4:89975800-89976800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr4:89975800-89976800	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr4:89975800-89976800	Enhancers	NH-A	brain
31	chr4:89975800-89977000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:89975800-89977000	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr4:89975800-89977000	Enhancers	NHEK	skin
34	chr4:89975800-89977200	Enhancers	Small Intestine	intestine
35	chr4:89975800-89978400	Active TSS	H1 Cell Line	embryonic stem cell
36	chr4:89975800-89978800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr4:89976000-89976800	Weak transcription	GM12878-XiMat	blood
38	chr4:89976000-89977200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr4:89976000-89978400	Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr4:89976000-89978800	Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr4:89976000-89978800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr4:89976000-89978800	Active TSS	Aorta	Aorta
43	chr4:89976000-89978800	Active TSS	Right Atrium	heart
44	chr4:89976200-89976600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:89976200-89976600	Flanking Active TSS	A549	lung
46	chr4:89976200-89976600	Enhancers	NHDF-Ad	bronchial
47	chr4:89976200-89976800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr4:89976200-89976800	Weak transcription	Fetal Muscle Leg	muscle
49	chr4:89976200-89976800	Weak transcription	Rectal Smooth Muscle	rectum
50	chr4:89976200-89977000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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