Variant report

Variant	rs3775498
Chromosome Location	chr4:147100117-147100118
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:147099369..147101389-chr4:147104400..147106028,2	MCF-7	breast:
2	chr4:147096699..147098795-chr4:147099511..147101268,2	MCF-7	breast:
3	chr4:147098952..147101592-chr4:147130358..147132148,2	K562	blood:

Variant related genes	Relation type
ENSG00000164167	Chromatin interaction

Extended variants
information (count: 102 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs10017509	0.84[CEU][hapmap]
rs10021707	0.81[YRI][hapmap]
rs10519776	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1079476	0.98[ASN][1000 genomes]
rs11100919	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11721367	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11721873	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11722991	0.84[CEU][hapmap]
rs11723069	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11724307	0.81[EUR][1000 genomes]
rs11728525	0.81[EUR][1000 genomes]
rs11728609	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11729787	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11730306	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11733347	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11734320	0.84[CEU][hapmap]
rs11940961	0.92[CEU][hapmap];0.82[CHB][hapmap]
rs12152657	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12152692	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12152709	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12186313	0.84[CEU][hapmap]
rs17021106	0.86[EUR][1000 genomes]
rs17021186	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17021188	0.86[LWK][hapmap]
rs17021217	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17021239	0.81[CEU][hapmap]
rs17021241	0.91[CEU][hapmap]
rs17756234	0.96[CEU][hapmap];1.00[CHB][hapmap];0.83[MEX][hapmap];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17757522	0.96[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.83[TSI][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17757685	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17757715	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17758092	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17758396	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17758420	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17814023	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17814065	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.81[TSI][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17814503	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17814598	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1864371	0.92[CEU][hapmap];0.82[CHB][hapmap]
rs1865531	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1865532	0.82[EUR][1000 genomes]
rs2068009	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2115796	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2115797	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2163171	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2164280	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28420466	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3733458	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3733459	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3733460	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3733461	0.84[CEU][hapmap]
rs3756081	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3756082	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3756083	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3815967	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4282199	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4835283	0.84[CEU][hapmap]
rs4835284	0.84[CEU][hapmap]
rs4835286	0.92[CEU][hapmap];0.82[CHB][hapmap];0.88[MEX][hapmap]
rs55736910	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56174047	0.81[EUR][1000 genomes]
rs56279747	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56333123	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56393662	0.98[ASN][1000 genomes]
rs62326797	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62326801	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62326802	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62326804	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62326848	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6537401	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6537402	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6537403	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6813969	0.81[CEU][hapmap]
rs6815527	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6816161	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6820462	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6821066	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6821444	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6821479	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6821863	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6824313	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6838174	0.83[CEU][hapmap]
rs6838458	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6839123	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.81[TSI][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6839141	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6843421	0.81[CEU][hapmap]
rs6844381	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6856647	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6858813	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72727944	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72727952	0.98[ASN][1000 genomes]
rs7356451	0.87[ASW][hapmap];1.00[YRI][hapmap]
rs7356484	0.87[ASW][hapmap];1.00[YRI][hapmap]
rs7657269	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7665079	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7745	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs919482	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs919483	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.83[TSI][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9308199	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][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	nsv461674	chr4:147047072-147143572	Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv595650	chr4:147047072-147143572	Genic enhancers Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1018859	chr4:147055618-147138397	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs3775498	LSM6	cis	cerebellar cortex	BrainEAC
rs3775498	LSM6	cis	parietal	SCAN
rs3775498	LSM6	cis	cerebellum	SCAN
rs3775498	RP11-6L6.2	cis	Nerve Tibial	GTEx
rs3775498	RP11-6L6.2	cis	Thyroid	GTEx
rs3775498	LSM6	cis	brain	BrainEAC
rs3775498	RP11-6L6.2	cis	Artery Tibial	GTEx
rs3775498	RP11-6L6.2	cis	Skin Sun Exposed Lower leg	GTEx
rs3775498	RP11-6L6.2	cis	Adipose Subcutaneous	GTEx
rs3775498	RP11-6L6.2	cis	Esophagus Muscularis	GTEx
rs3775498	RP11-6L6.2	cis	lung	GTEx

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147097600-147108800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:147097800-147101400	Enhancers	Primary B cells from peripheral blood	blood
3	chr4:147097800-147104200	Weak transcription	Placenta	Placenta
4	chr4:147097800-147104600	Weak transcription	Fetal Muscle Trunk	muscle
5	chr4:147097800-147108600	Weak transcription	HSMMtube	muscle
6	chr4:147097800-147108800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:147097800-147108800	Weak transcription	Esophagus	oesophagus
8	chr4:147097800-147111000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr4:147097800-147115400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:147098000-147102200	Enhancers	Fetal Heart	heart
11	chr4:147098000-147102800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr4:147098200-147101000	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr4:147098200-147101200	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr4:147098200-147102000	Enhancers	Brain Hippocampus Middle	brain
15	chr4:147098400-147100200	Enhancers	Primary T cells fromperipheralblood	blood
16	chr4:147098400-147100600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr4:147098400-147100600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr4:147098400-147100600	Weak transcription	Fetal Brain Female	brain
19	chr4:147098400-147100800	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr4:147098400-147100800	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr4:147098400-147100800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:147098400-147100800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:147098400-147100800	Weak transcription	Duodenum Mucosa	Duodenum
24	chr4:147098400-147101000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr4:147098400-147101000	Enhancers	Brain Anterior Caudate	brain
26	chr4:147098400-147101200	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr4:147098400-147101400	Enhancers	HepG2	liver
28	chr4:147098400-147101600	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr4:147098400-147101600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr4:147098400-147102000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr4:147098400-147102200	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr4:147098400-147102400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr4:147098400-147102600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr4:147098400-147103200	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr4:147098400-147103600	Weak transcription	A549	lung
36	chr4:147098400-147104200	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr4:147098400-147104400	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr4:147098400-147107400	Weak transcription	HSMM	muscle
39	chr4:147098400-147107800	Weak transcription	Fetal Kidney	kidney
40	chr4:147098400-147108000	Weak transcription	NH-A	brain
41	chr4:147098400-147108800	Weak transcription	NHLF	lung
42	chr4:147098400-147111400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr4:147098400-147118600	Weak transcription	Colonic Mucosa	Colon
44	chr4:147098600-147100200	Weak transcription	NHEK	skin
45	chr4:147098600-147100600	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr4:147098600-147100800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:147098600-147101000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr4:147098600-147101000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr4:147098600-147101000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr4:147098600-147101000	Weak transcription	Stomach Mucosa	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links