Variant report

Variant	rs7649081
Chromosome Location	chr3:46747192-46747193
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:46746749..46747355-chr3:47039353..47040339,2	MCF-7	breast:
2	chr3:46746279..46747291-chr3:46951057..46951891,3	MCF-7	breast:
3	chr3:46746240..46747607-chr3:46936343..46937490,8	K562	blood:
4	chr3:46745401..46748199-chr3:46947346..46950114,2	K562	blood:
5	chr3:46476162..46478897-chr3:46745088..46748069,2	K562	blood:
6	chr3:46746642..46747266-chr3:46889901..46890658,2	MCF-7	breast:
7	chr3:46742077..46744445-chr3:46744916..46748199,4	K562	blood:

Variant related genes	Relation type
ENSG00000181585	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs12492868	0.86[ASN][1000 genomes]
rs12496585	0.88[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs34190208	0.89[ASN][1000 genomes]
rs34788938	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4076927	0.82[CHB][hapmap];0.84[CHD][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs4682825	0.81[JPT][hapmap]
rs55650397	0.88[ASN][1000 genomes]
rs55665753	0.84[ASN][1000 genomes]
rs55986901	0.84[ASN][1000 genomes]
rs56313683	0.91[ASN][1000 genomes]
rs56375912	0.84[ASN][1000 genomes]
rs56670151	0.90[ASN][1000 genomes]
rs59191033	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs62246210	0.86[ASN][1000 genomes]
rs6442020	0.82[CHB][hapmap];0.84[CHD][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs6442024	0.84[ASN][1000 genomes]
rs6768252	0.85[GIH][hapmap]
rs6804514	0.84[ASN][1000 genomes]
rs7372799	0.82[CHB][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs7373358	0.87[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs73831197	0.91[ASN][1000 genomes]
rs7426833	0.82[CHB][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs7610936	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7613489	0.82[CHB][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs7633016	0.82[CHB][hapmap];0.84[CHD][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs7634963	0.88[CHB][hapmap];0.94[CHD][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs7642448	0.82[CHB][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs7642783	0.94[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.89[ASN][1000 genomes]
rs7649029	0.84[ASN][1000 genomes]
rs7650366	0.94[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007449	chr3:46652343-46986578	Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	nsv536554	chr3:46652343-46986578	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv876740	chr3:46656980-46748453	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv876741	chr3:46663372-46763839	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv516623	chr3:46680063-46852679	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
6	esv2757869	chr3:46680452-46972489	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
7	esv2759147	chr3:46680452-46972489	Genic enhancers Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
8	esv1804680	chr3:46704348-46869911	Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
9	nsv876742	chr3:46705369-46763839	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
10	nsv536555	chr3:46706571-46817963	Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv536556	chr3:46706571-46849443	Genic enhancers Bivalent/Poised TSS Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
12	nsv536557	chr3:46706571-46853434	Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
13	nsv536558	chr3:46706571-47024756	Enhancers Bivalent Enhancer Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
14	esv1797503	chr3:46708712-46760713	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
15	nsv876743	chr3:46716523-46753577	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
16	nsv876744	chr3:46716523-46763839	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
17	nsv460525	chr3:46728659-46790397	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	17 gene(s)	inside rSNPs	diseases
18	nsv590179	chr3:46728659-46790397	Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	17 gene(s)	inside rSNPs	diseases
19	esv1847964	chr3:46729757-46753976	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46742800-46748000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:46743400-46752600	Weak transcription	Left Ventricle	heart
3	chr3:46743400-46758800	Weak transcription	Lung	lung
4	chr3:46743600-46749000	Weak transcription	Psoas Muscle	Psoas
5	chr3:46743600-46750000	Weak transcription	Primary T cells from cord blood	blood
6	chr3:46743600-46752200	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr3:46744000-46755800	Weak transcription	Brain Germinal Matrix	brain
8	chr3:46744000-46792200	Weak transcription	Right Atrium	heart
9	chr3:46744400-46750000	Weak transcription	Fetal Brain Male	brain
10	chr3:46744400-46750200	Weak transcription	Fetal Brain Female	brain
11	chr3:46744400-46757400	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr3:46746200-46747400	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr3:46746400-46747200	Enhancers	Liver	Liver
14	chr3:46746400-46747600	Enhancers	Fetal Intestine Large	intestine
15	chr3:46746400-46747800	Enhancers	Fetal Intestine Small	intestine
16	chr3:46746400-46749600	Enhancers	Placenta Amnion	Placenta Amnion
17	chr3:46746400-46751000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr3:46746600-46747200	Enhancers	Spleen	Spleen
19	chr3:46746600-46748000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr3:46746600-46748000	Enhancers	Adipose Nuclei	Adipose
21	chr3:46746600-46748600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr3:46746600-46748800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr3:46746600-46748800	Enhancers	Fetal Muscle Leg	muscle
24	chr3:46746600-46750000	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr3:46746800-46747600	Enhancers	Fetal Heart	heart
26	chr3:46746800-46747800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr3:46746800-46748000	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr3:46746800-46748200	Enhancers	NH-A	brain
29	chr3:46746800-46748400	Bivalent Enhancer	Placenta	Placenta
30	chr3:46746800-46748400	Enhancers	HUVEC	blood vessel
31	chr3:46746800-46748600	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr3:46746800-46748800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr3:46746800-46748800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr3:46746800-46748800	Bivalent Enhancer	Fetal Stomach	stomach
35	chr3:46746800-46749000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr3:46746800-46749000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr3:46746800-46749000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr3:46746800-46749200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr3:46746800-46750600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr3:46747000-46747400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
41	chr3:46747000-46748000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr3:46747000-46748200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr3:46747000-46748200	Enhancers	HSMM	muscle
44	chr3:46747000-46748200	Enhancers	HSMMtube	muscle
45	chr3:46747000-46750200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr3:46747000-46750600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr3:46747000-46750800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr3:46747000-46751000	Weak transcription	Ovary	ovary
49	chr3:46747000-46753000	Weak transcription	Right Ventricle	heart
50	chr3:46747000-46755000	Weak transcription	Brain Cingulate Gyrus	brain

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