Variant report

Variant	rs34095418
Chromosome Location	chr5:178593899-178593900
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:178593807..178594987-chr5:178687910..178688845,5	MCF-7	breast:
2	chr5:178593773..178595177-chr5:178920715..178921686,6	MCF-7	breast:

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11960126	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6899233	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7706427	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024560	chr5:178415364-178917595	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv537975	chr5:178415364-178917595	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv817413	chr5:178415365-179020558	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
4	nsv1033597	chr5:178423101-178752095	Strong transcription Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1031829	chr5:178442633-178658706	Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv482750	chr5:178482653-178663586	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1026790	chr5:178511268-178687428	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv482352	chr5:178525060-178697496	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv883222	chr5:178540975-178595870	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
10	nsv1016097	chr5:178544084-178866001	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv1026968	chr5:178545479-178865895	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv537976	chr5:178545479-178865895	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
13	nsv600496	chr5:178552518-178752351	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
14	nsv883223	chr5:178576631-178630445	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178567000-178594000	Weak transcription	Gastric	stomach
2	chr5:178582000-178594000	Weak transcription	NHLF	lung
3	chr5:178583000-178594000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr5:178586400-178594400	Weak transcription	Fetal Lung	lung
5	chr5:178586600-178594000	Weak transcription	HSMMtube	muscle
6	chr5:178588200-178594000	Weak transcription	HSMM	muscle
7	chr5:178590000-178594000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr5:178590000-178594000	Weak transcription	Fetal Intestine Small	intestine
9	chr5:178590400-178594000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr5:178590400-178594000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr5:178591400-178594000	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr5:178591800-178594200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr5:178592400-178594000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr5:178592400-178594600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr5:178593600-178594000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr5:178593600-178594200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr5:178593800-178594000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr5:178593800-178594000	Enhancers	Primary B cells from peripheral blood	blood
19	chr5:178593800-178594000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr5:178593800-178594000	Enhancers	Primary hematopoietic stem cells	blood
21	chr5:178593800-178594000	Active TSS	Primary T regulatory cells fromperipheralblood	blood
22	chr5:178593800-178594000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr5:178593800-178594000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr5:178593800-178594000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr5:178593800-178594000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
26	chr5:178593800-178594000	Enhancers	Adipose Nuclei	Adipose
27	chr5:178593800-178594000	Enhancers	Brain Cingulate Gyrus	brain
28	chr5:178593800-178594000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
29	chr5:178593800-178594000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
30	chr5:178593800-178594000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
31	chr5:178593800-178594000	Enhancers	Ovary	ovary
32	chr5:178593800-178594000	Active TSS	Osteobl	bone
33	chr5:178593800-178594200	Enhancers	H1 Cell Line	embryonic stem cell
34	chr5:178593800-178594200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
35	chr5:178593800-178594400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr5:178593800-178594400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
37	chr5:178593800-178594400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
38	chr5:178593800-178594400	Active TSS	Brain Substantia Nigra	brain
39	chr5:178593800-178594400	Active TSS	Duodenum Smooth Muscle	Duodenum
40	chr5:178593800-178594400	Active TSS	Thymus	Thymus
41	chr5:178593800-178594400	Enhancers	Spleen	Spleen
42	chr5:178593800-178594400	Enhancers	NHDF-Ad	bronchial
43	chr5:178593800-178594600	Active TSS	Brain Angular Gyrus	brain
44	chr5:178593800-178594600	Enhancers	Colonic Mucosa	Colon
45	chr5:178593800-178594600	Enhancers	Placenta	Placenta
46	chr5:178593800-178594600	Active TSS	Rectal Smooth Muscle	rectum
47	chr5:178593800-178594800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr5:178593800-178594800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr5:178593800-178594800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
50	chr5:178593800-178595000	Bivalent Enhancer	Fetal Stomach	stomach

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