Variant report

Variant	rs56335325
Chromosome Location	chr7:5272638-5272639
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	chr7:5272109..5273708-chr7:5323100..5324631,2	MCF-7	breast:
2	chr7:5263758..5266734-chr7:5271023..5272785,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000157954	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs41280684	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55698647	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57418885	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73046123	0.81[EUR][1000 genomes]
rs73046135	0.85[AFR][1000 genomes];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73046149	0.85[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs7785898	0.86[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530968	chr7:4572250-5418004	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv869165	chr7:4889618-5799719	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	352 gene(s)	inside rSNPs	diseases
3	nsv530979	chr7:5101631-5864814	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
4	nsv916396	chr7:5128917-5370805	Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	nsv530981	chr7:5157150-5920006	Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	348 gene(s)	inside rSNPs	diseases
6	nsv887390	chr7:5224407-5411296	Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv887391	chr7:5224407-5572132	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	292 gene(s)	inside rSNPs	diseases
8	nsv830889	chr7:5248157-5427465	Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
9	nsv8034	chr7:5257953-5417973	Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
10	nsv887392	chr7:5263194-5359680	Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5231400-5279800	Weak transcription	Fetal Brain Male	brain
2	chr7:5231800-5273400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:5234000-5274800	Weak transcription	Stomach Mucosa	stomach
4	chr7:5237400-5273400	Strong transcription	Dnd41	blood
5	chr7:5248400-5273200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:5249000-5272800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:5249000-5272800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr7:5249000-5273000	Strong transcription	Muscle Satellite Cultured Cells	--
9	chr7:5249000-5273200	Strong transcription	Fetal Muscle Trunk	muscle
10	chr7:5249000-5273600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr7:5249000-5273600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
12	chr7:5249200-5272800	Strong transcription	Skeletal Muscle Female	skeletal muscle
13	chr7:5249200-5273000	Strong transcription	Stomach Smooth Muscle	stomach
14	chr7:5249200-5273400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:5249200-5273400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr7:5249200-5273400	Strong transcription	Duodenum Smooth Muscle	Duodenum
17	chr7:5249200-5273400	Strong transcription	Fetal Stomach	stomach
18	chr7:5249200-5273400	Strong transcription	Skeletal Muscle Male	skeletal muscle
19	chr7:5249200-5273600	Strong transcription	Fetal Intestine Small	intestine
20	chr7:5249600-5272800	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr7:5249600-5273400	Strong transcription	Right Ventricle	heart
22	chr7:5249800-5273600	Strong transcription	Fetal Brain Female	brain
23	chr7:5250800-5272800	Strong transcription	Liver	Liver
24	chr7:5254000-5272800	Strong transcription	Brain Germinal Matrix	brain
25	chr7:5254000-5273400	Strong transcription	Cortex derived primary cultured neurospheres	brain
26	chr7:5254000-5273400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr7:5254200-5280000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr7:5254600-5273600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr7:5258000-5279600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr7:5259000-5273000	Strong transcription	Primary neutrophils fromperipheralblood	blood
31	chr7:5261000-5273400	Strong transcription	Colon Smooth Muscle	Colon
32	chr7:5261800-5273400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr7:5262000-5273000	Strong transcription	NHLF	lung
34	chr7:5262400-5272800	Strong transcription	Aorta	Aorta
35	chr7:5262400-5273000	Strong transcription	Pancreas	Pancrea
36	chr7:5262400-5273400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr7:5262400-5273400	Strong transcription	Gastric	stomach
38	chr7:5266400-5272800	Strong transcription	NHEK	skin
39	chr7:5266600-5276200	Weak transcription	Fetal Kidney	kidney
40	chr7:5267400-5279800	Weak transcription	Right Atrium	heart
41	chr7:5268200-5273000	Strong transcription	Fetal Intestine Large	intestine
42	chr7:5268200-5273400	Strong transcription	Thymus	Thymus
43	chr7:5268200-5280000	Weak transcription	Psoas Muscle	Psoas
44	chr7:5269200-5272800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr7:5269200-5273400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr7:5269400-5273400	Genic enhancers	Spleen	Spleen
47	chr7:5269800-5273200	Genic enhancers	Fetal Thymus	thymus
48	chr7:5269800-5274800	Weak transcription	K562	blood
49	chr7:5270000-5273000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr7:5270200-5272800	Strong transcription	Brain Inferior Temporal Lobe	brain

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