Variant report

Variant	rs11078396
Chromosome Location	chr17:17647396-17647397
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:17583280..17588870-chr17:17641850..17648309,13	MCF-7	breast:
2	chr17:17643501..17645384-chr17:17646816..17648997,3	MCF-7	breast:
3	chr17:17583806..17586953-chr17:17646160..17649545,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000108557	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11078397	1.00[CEU][hapmap];1.00[GIH][hapmap];0.85[TSI][hapmap];0.96[EUR][1000 genomes]
rs11651378	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs11651383	0.96[EUR][1000 genomes]
rs11652525	0.96[EUR][1000 genomes]
rs11652656	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs11653007	1.00[CEU][hapmap]
rs11653424	0.80[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.85[TSI][hapmap];0.83[YRI][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11653696	1.00[CEU][hapmap];0.85[GIH][hapmap];0.85[TSI][hapmap];0.96[EUR][1000 genomes]
rs11654482	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs11656769	1.00[CEU][hapmap];0.85[GIH][hapmap];0.85[TSI][hapmap];0.89[EUR][1000 genomes]
rs11658846	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs11659047	0.85[GIH][hapmap];0.87[TSI][hapmap]
rs12103565	1.00[CHB][hapmap];0.96[ASN][1000 genomes]
rs12603026	0.83[ASN][1000 genomes]
rs12603397	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4925112	1.00[CEU][hapmap]
rs56022233	0.96[EUR][1000 genomes]
rs60149982	0.96[EUR][1000 genomes]
rs60549849	0.96[EUR][1000 genomes]
rs60889477	0.94[EUR][1000 genomes]
rs6502612	0.81[EUR][1000 genomes]
rs7217764	0.85[GIH][hapmap]
rs7219568	0.85[GIH][hapmap]
rs7222358	0.85[GIH][hapmap]
rs7224725	0.85[GIH][hapmap]
rs73295691	0.96[EUR][1000 genomes]
rs73295697	1.00[ASN][1000 genomes]
rs73295699	0.94[EUR][1000 genomes]
rs8066159	1.00[CEU][hapmap];0.85[TSI][hapmap];0.94[EUR][1000 genomes]
rs8066177	1.00[CEU][hapmap];0.85[TSI][hapmap];0.94[EUR][1000 genomes]
rs8079880	0.90[EUR][1000 genomes]
rs9897362	0.85[GIH][hapmap]
rs9910075	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv907748	chr17:17412032-17782404	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
2	nsv1065270	chr17:17430116-17823086	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
3	nsv543236	chr17:17430116-17823086	Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
4	nsv907752	chr17:17569012-17750907	Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
5	nsv531183	chr17:17571035-18205309	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
6	nsv907753	chr17:17573539-17747289	Genic enhancers Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
7	nsv907754	chr17:17573539-17782404	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
8	nsv1061126	chr17:17578826-17803194	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
9	nsv543238	chr17:17578826-17803194	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
10	nsv833385	chr17:17594037-17765578	Enhancers Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription 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 miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
11	nsv1058884	chr17:17594370-17803194	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
12	nsv543240	chr17:17594370-17803194	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
13	nsv543241	chr17:17596222-17703059	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
14	nsv1064176	chr17:17596222-17803194	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
15	nsv543242	chr17:17596222-17803194	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
16	nsv1062361	chr17:17598407-17746899	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
17	nsv543243	chr17:17598407-17746899	Genic enhancers Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
18	nsv907756	chr17:17619859-17747289	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
19	nsv522668	chr17:17619859-17752809	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
20	nsv907757	chr17:17619859-17752809	Flanking Bivalent TSS/Enh Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
21	nsv907758	chr17:17619859-17782404	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
22	nsv907759	chr17:17619859-17802478	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
23	nsv532109	chr17:17630064-17700497	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
24	nsv1059949	chr17:17632590-17803194	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
25	nsv543244	chr17:17632590-17803194	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17636200-17648200	Weak transcription	Dnd41	blood
2	chr17:17639000-17647600	Enhancers	Left Ventricle	heart
3	chr17:17640400-17647400	Enhancers	Right Ventricle	heart
4	chr17:17640600-17647800	Enhancers	Pancreas	Pancrea
5	chr17:17641600-17652200	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr17:17642200-17650600	Weak transcription	GM12878-XiMat	blood
7	chr17:17642600-17652400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr17:17642800-17651400	Weak transcription	Primary B cells from peripheral blood	blood
9	chr17:17643200-17655200	Weak transcription	Aorta	Aorta
10	chr17:17643600-17652200	Weak transcription	Psoas Muscle	Psoas
11	chr17:17643600-17654600	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr17:17643800-17652400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr17:17644200-17649200	Weak transcription	Primary T cells from cord blood	blood
14	chr17:17644200-17654200	Weak transcription	HepG2	liver
15	chr17:17644600-17648200	Weak transcription	Hela-S3	cervix
16	chr17:17644600-17649200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr17:17644800-17649200	Weak transcription	Gastric	stomach
18	chr17:17644800-17651800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr17:17644800-17653000	Weak transcription	Small Intestine	intestine
20	chr17:17645000-17647400	Enhancers	Right Atrium	heart
21	chr17:17645000-17648200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr17:17645000-17649000	Weak transcription	Thymus	Thymus
23	chr17:17645000-17649400	Weak transcription	Fetal Thymus	thymus
24	chr17:17645000-17652000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr17:17645000-17652200	Weak transcription	Primary hematopoietic stem cells	blood
26	chr17:17645200-17652600	Weak transcription	Duodenum Mucosa	Duodenum
27	chr17:17645400-17648000	Enhancers	Brain Hippocampus Middle	brain
28	chr17:17645400-17648200	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr17:17645400-17648400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr17:17645400-17648600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr17:17645400-17649000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr17:17645400-17649200	Enhancers	Brain Substantia Nigra	brain
33	chr17:17645400-17650600	Weak transcription	Colonic Mucosa	Colon
34	chr17:17645400-17652000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr17:17645400-17652600	Enhancers	Brain Cingulate Gyrus	brain
36	chr17:17645400-17655000	Enhancers	Brain Angular Gyrus	brain
37	chr17:17645600-17647600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr17:17645600-17649000	Weak transcription	Esophagus	oesophagus
39	chr17:17645600-17649000	Weak transcription	Lung	lung
40	chr17:17645600-17649200	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr17:17645600-17649200	Weak transcription	Fetal Intestine Large	intestine
42	chr17:17645600-17652000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr17:17645600-17652000	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr17:17645600-17652200	Strong transcription	Fetal Intestine Small	intestine
45	chr17:17645600-17652600	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr17:17645600-17652600	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr17:17645600-17654800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr17:17645800-17649200	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr17:17645800-17649600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr17:17645800-17650200	Weak transcription	NHEK	skin

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