Variant report

Variant	rs6762331
Chromosome Location	chr3:140961822-140961823
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:140960420..140963104-chr3:140988791..140990296,2	K562	blood:
2	chr3:140949314..140952650-chr3:140959989..140963598,3	MCF-7	breast:
3	chr3:140960166..140963166-chr3:140967948..140970939,3	MCF-7	breast:
4	chr3:140961342..140963212-chr3:140979799..140982645,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000155893	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11556022	1.00[JPT][hapmap]
rs11710222	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11713226	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.84[ASN][1000 genomes]
rs11713257	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.84[ASN][1000 genomes]
rs16851191	0.94[CEU][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16851272	0.82[CEU][hapmap]
rs2292401	0.82[EUR][1000 genomes]
rs2292402	0.83[EUR][1000 genomes]
rs4683587	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4683589	0.81[ASN][1000 genomes]
rs55694384	0.81[ASN][1000 genomes]
rs55923220	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56163421	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56254804	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57562453	0.81[ASN][1000 genomes]
rs6439986	0.84[EUR][1000 genomes]
rs6439987	0.84[EUR][1000 genomes]
rs6439989	0.94[CEU][hapmap];0.90[CHB][hapmap];0.95[EUR][1000 genomes]
rs6794495	1.00[JPT][hapmap]
rs72994962	0.84[ASN][1000 genomes]
rs72994967	0.84[ASN][1000 genomes]
rs73869537	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7618821	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7629005	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7636976	0.83[EUR][1000 genomes]
rs9682606	0.88[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460870	chr3:140938546-141005574	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv591892	chr3:140938546-141005574	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140951600-140979000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr3:140951800-140962000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:140951800-140962200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:140952000-140962000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr3:140955200-140962000	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr3:140955200-140980600	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr3:140955400-140968400	Genic enhancers	Dnd41	blood
8	chr3:140955400-140985800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr3:140956200-140962600	Enhancers	Fetal Brain Male	brain
10	chr3:140956400-140962600	Genic enhancers	Thymus	Thymus
11	chr3:140956600-140962600	Enhancers	Primary T cells fromperipheralblood	blood
12	chr3:140956600-140962600	Enhancers	Fetal Muscle Leg	muscle
13	chr3:140956600-140962600	Enhancers	Left Ventricle	heart
14	chr3:140957000-140962200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr3:140957400-140962000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr3:140957400-140967800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr3:140957400-140967800	Weak transcription	Gastric	stomach
18	chr3:140957400-141001000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr3:140957800-140962000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr3:140957800-140973600	Weak transcription	Brain Hippocampus Middle	brain
21	chr3:140958000-140962600	Enhancers	Right Atrium	heart
22	chr3:140958400-140962000	Enhancers	Brain Anterior Caudate	brain
23	chr3:140958400-140962200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr3:140958600-140962200	Enhancers	Lung	lung
25	chr3:140958600-140962400	Enhancers	Psoas Muscle	Psoas
26	chr3:140958800-140962200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr3:140958800-140962400	Enhancers	Osteobl	bone
28	chr3:140959000-140962200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr3:140959000-140962200	Enhancers	NHEK	skin
30	chr3:140959000-140962600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr3:140959000-140962600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr3:140959000-140962600	Enhancers	Muscle Satellite Cultured Cells	--
33	chr3:140959000-140962600	Enhancers	NH-A	brain
34	chr3:140959200-140962000	Enhancers	HSMM	muscle
35	chr3:140959200-140962400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr3:140959200-140962600	Enhancers	Fetal Muscle Trunk	muscle
37	chr3:140959200-140966200	Enhancers	Fetal Heart	heart
38	chr3:140959200-140998400	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr3:140959400-140962000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr3:140959400-140964800	Weak transcription	Pancreas	Pancrea
41	chr3:140959400-140965200	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr3:140959600-140962200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr3:140959600-140962200	Weak transcription	K562	blood
44	chr3:140959800-140962000	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr3:140959800-140962600	Enhancers	Fetal Intestine Large	intestine
46	chr3:140959800-140964400	Weak transcription	HepG2	liver
47	chr3:140960000-140980000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr3:140960200-140962000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr3:140960200-140962000	Enhancers	Spleen	Spleen
50	chr3:140960400-140962200	Weak transcription	H1 Cell Line	embryonic stem cell

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