Variant report

Variant	rs7796922
Chromosome Location	chr7:33171110-33171111
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:33169914..33172476-chr7:33187197..33189119,2	MCF-7	breast:

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs1019301	0.82[ASN][1000 genomes]
rs10269945	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10274959	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10486523	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10486525	0.82[ASN][1000 genomes]
rs1362370	0.82[ASN][1000 genomes]
rs17169807	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17169808	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17170099	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17170104	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17170105	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17170120	0.82[ASN][1000 genomes]
rs17170131	0.82[ASN][1000 genomes]
rs17170138	0.82[ASN][1000 genomes]
rs17170140	0.82[ASN][1000 genomes]
rs17170143	0.82[ASN][1000 genomes]
rs17170155	0.82[ASN][1000 genomes]
rs17170167	0.80[ASN][1000 genomes]
rs17170169	0.80[ASN][1000 genomes]
rs17170173	0.80[ASN][1000 genomes]
rs17170178	0.80[ASN][1000 genomes]
rs1833176	0.80[ASN][1000 genomes]
rs2392229	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34950347	0.82[ASN][1000 genomes]
rs3750122	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3828996	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4538777	0.82[ASN][1000 genomes]
rs4628178	0.82[ASN][1000 genomes]
rs55847945	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55865959	0.82[ASN][1000 genomes]
rs55924837	0.80[ASN][1000 genomes]
rs56195645	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56343904	0.80[ASN][1000 genomes]
rs58550767	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59075362	0.82[ASN][1000 genomes]
rs59446325	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60268357	0.82[ASN][1000 genomes]
rs60491621	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6943198	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6944559	0.82[ASN][1000 genomes]
rs6952244	0.82[ASN][1000 genomes]
rs6969284	0.82[ASN][1000 genomes]
rs6973552	0.82[ASN][1000 genomes]
rs73307386	0.82[ASN][1000 genomes]
rs73307398	0.82[ASN][1000 genomes]
rs73307400	0.82[ASN][1000 genomes]
rs73307578	0.82[AFR][1000 genomes]
rs73307587	0.82[AFR][1000 genomes]
rs73307592	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73309308	0.82[ASN][1000 genomes]
rs73309310	0.82[ASN][1000 genomes]
rs73309316	0.82[ASN][1000 genomes]
rs73309318	0.82[ASN][1000 genomes]
rs73309324	0.82[ASN][1000 genomes]
rs73309326	0.82[ASN][1000 genomes]
rs73309328	0.82[ASN][1000 genomes]
rs73309405	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73309423	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73313121	0.80[ASN][1000 genomes]
rs73313134	0.80[ASN][1000 genomes]
rs73313138	0.80[ASN][1000 genomes]
rs73317492	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73319406	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73319407	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73319408	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73688093	0.82[ASN][1000 genomes]
rs73689881	0.82[ASN][1000 genomes]
rs7459365	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7781504	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7793667	0.82[ASN][1000 genomes]
rs7795704	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7798118	0.82[ASN][1000 genomes]
rs7799346	0.82[ASN][1000 genomes]
rs7808472	0.82[ASN][1000 genomes]
rs9791555	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9791901	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029220	chr7:32921484-33262190	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
2	nsv830942	chr7:33048075-33246735	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv508450	chr7:33123335-33184848	Flanking Active TSS Strong transcription Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1033502	chr7:33124005-33185470	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1025361	chr7:33125663-33185470	Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv869720	chr7:33127192-33193580	Flanking Active TSS Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv1026615	chr7:33128234-33185470	Genic enhancers Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS 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	12 gene(s)	inside rSNPs	diseases
8	nsv1020741	chr7:33130675-33185470	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	nsv1027807	chr7:33130675-33190591	Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	esv2761318	chr7:33130687-33185482	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	nsv464422	chr7:33131729-33187279	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
12	nsv606606	chr7:33131729-33187279	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
13	nsv606607	chr7:33131729-33192502	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
14	nsv464423	chr7:33131729-33192800	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
15	nsv606608	chr7:33131729-33192800	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
16	nsv520406	chr7:33131729-33192837	Enhancers Strong transcription Active TSS Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
17	nsv606609	chr7:33131729-33196354	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
18	nsv1030007	chr7:33132814-33185470	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers 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	12 gene(s)	inside rSNPs	diseases
19	nsv1028637	chr7:33133742-33185470	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
20	nsv830943	chr7:33167106-33352759	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
21	nsv933681	chr7:33169539-33185909	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
22	nsv933792	chr7:33169693-33216984	ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
23	nsv532119	chr7:33169715-33186579	Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33170000-33176800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:33170000-33178400	Weak transcription	Left Ventricle	heart
3	chr7:33170200-33171200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:33170200-33171200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr7:33170200-33171200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr7:33170200-33171200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr7:33170200-33171200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr7:33170200-33171200	Enhancers	Colon Smooth Muscle	Colon
9	chr7:33170200-33171200	Weak transcription	Right Atrium	heart
10	chr7:33170200-33171200	Enhancers	HepG2	liver
11	chr7:33170200-33171400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:33170200-33171400	Enhancers	Duodenum Mucosa	Duodenum
13	chr7:33170200-33171600	Enhancers	Fetal Brain Female	brain
14	chr7:33170200-33171800	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr7:33170200-33171800	Enhancers	Brain Cingulate Gyrus	brain
16	chr7:33170200-33171800	Enhancers	Fetal Lung	lung
17	chr7:33170200-33172000	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr7:33170200-33173400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:33170200-33175200	Weak transcription	Fetal Muscle Trunk	muscle
20	chr7:33170200-33182000	Weak transcription	Primary hematopoietic stem cells	blood
21	chr7:33170200-33185000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr7:33170200-33188400	Weak transcription	Psoas Muscle	Psoas
23	chr7:33170200-33205800	Weak transcription	Aorta	Aorta
24	chr7:33170400-33171200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:33170400-33171200	Enhancers	Fetal Stomach	stomach
26	chr7:33170600-33171200	Flanking Active TSS	Brain Anterior Caudate	brain
27	chr7:33170600-33172000	Enhancers	Fetal Brain Male	brain
28	chr7:33170800-33171200	Flanking Active TSS	Brain Germinal Matrix	brain
29	chr7:33170800-33171200	Flanking Active TSS	Brain Hippocampus Middle	brain
30	chr7:33170800-33171200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
31	chr7:33170800-33171200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
32	chr7:33170800-33171200	Enhancers	Stomach Smooth Muscle	stomach
33	chr7:33170800-33171200	Flanking Active TSS	Dnd41	blood
34	chr7:33170800-33171200	Enhancers	NH-A	brain
35	chr7:33171000-33171200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr7:33171000-33171200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr7:33171000-33171200	Enhancers	Fetal Intestine Large	intestine
38	chr7:33171000-33171800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr7:33171000-33171800	Enhancers	Brain Angular Gyrus	brain
40	chr7:33171000-33171800	Weak transcription	Fetal Kidney	kidney
41	chr7:33171000-33172000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr7:33171000-33172000	Enhancers	Brain Substantia Nigra	brain
43	chr7:33171000-33173400	Weak transcription	Primary T helper cells PMA-I stimulated	--
44	chr7:33171000-33175200	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr7:33171000-33176800	Weak transcription	Ovary	ovary
46	chr7:33171000-33182200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr7:33171000-33184000	Weak transcription	Skeletal Muscle Female	skeletal muscle

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