Variant report

Variant	rs73773854
Chromosome Location	chr5:95214745-95214746
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	chr5:95206364..95208492-chr5:95212828..95215499,2	MCF-7	breast:
2	chr5:95213765..95215315-chr5:95296484..95298680,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000251314	Chromatin interaction
ENSG00000118985	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs28926199	1.00[AMR][1000 genomes]
rs4330485	1.00[AMR][1000 genomes]
rs55652330	1.00[AMR][1000 genomes]
rs55757346	1.00[AMR][1000 genomes]
rs57217517	1.00[AMR][1000 genomes]
rs57808386	1.00[AMR][1000 genomes]
rs58292647	1.00[AMR][1000 genomes]
rs59433710	1.00[AMR][1000 genomes]
rs60897703	1.00[AMR][1000 genomes]
rs61572029	1.00[AMR][1000 genomes]
rs6870381	1.00[AMR][1000 genomes]
rs73771803	1.00[AMR][1000 genomes]
rs73771806	1.00[AMR][1000 genomes]
rs73771809	1.00[AMR][1000 genomes]
rs73771826	1.00[AMR][1000 genomes]
rs73771828	1.00[AMR][1000 genomes]
rs73771831	1.00[AMR][1000 genomes]
rs73771837	1.00[AMR][1000 genomes]
rs73771838	1.00[AMR][1000 genomes]
rs73771843	1.00[AMR][1000 genomes]
rs73773855	1.00[AMR][1000 genomes]
rs73780154	1.00[AMR][1000 genomes]
rs7705187	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015180	chr5:95134357-95286446	Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1019566	chr5:95180352-95300677	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Genic enhancers 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	25 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	chr5:95195200-95217400	Weak transcription	Brain Cingulate Gyrus	brain
2	chr5:95202800-95217200	Weak transcription	Brain Hippocampus Middle	brain
3	chr5:95206600-95218800	Weak transcription	HSMM	muscle
4	chr5:95206800-95217400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr5:95207400-95218000	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr5:95207400-95219000	Weak transcription	Psoas Muscle	Psoas
7	chr5:95208800-95217600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr5:95210200-95220000	Weak transcription	Right Ventricle	heart
9	chr5:95210600-95221800	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr5:95211000-95218400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr5:95212000-95216800	Enhancers	Liver	Liver
12	chr5:95212000-95224000	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr5:95212400-95223800	Weak transcription	Brain Substantia Nigra	brain
14	chr5:95212600-95219800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr5:95213000-95215400	Weak transcription	Gastric	stomach
16	chr5:95213000-95244600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr5:95213800-95215400	Enhancers	Fetal Intestine Small	intestine
18	chr5:95213800-95215800	Enhancers	GM12878-XiMat	blood
19	chr5:95214000-95214800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr5:95214000-95214800	Enhancers	K562	blood
21	chr5:95214000-95215800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:95214000-95216200	Flanking Active TSS	HepG2	liver
23	chr5:95214000-95216600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr5:95214000-95216600	Enhancers	Fetal Intestine Large	intestine
25	chr5:95214000-95219200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr5:95214200-95214800	Enhancers	Fetal Heart	heart
27	chr5:95214200-95215600	Enhancers	Rectal Mucosa Donor 29	rectum
28	chr5:95214200-95215600	Enhancers	Stomach Mucosa	stomach
29	chr5:95214200-95215800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr5:95214200-95216200	Enhancers	Placenta	Placenta
31	chr5:95214200-95217800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr5:95214200-95218000	Enhancers	NHEK	skin
33	chr5:95214200-95219000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr5:95214400-95214800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr5:95214400-95214800	Enhancers	Right Atrium	heart
36	chr5:95214400-95215000	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr5:95214400-95215200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr5:95214400-95215200	Weak transcription	Esophagus	oesophagus
39	chr5:95214400-95215200	Enhancers	A549	lung
40	chr5:95214400-95216000	Enhancers	HMEC	breast
41	chr5:95214400-95216200	Weak transcription	Colonic Mucosa	Colon
42	chr5:95214400-95216400	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr5:95214400-95216800	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr5:95214400-95224800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr5:95214400-95234200	Weak transcription	Fetal Brain Female	brain
46	chr5:95214400-95247800	Weak transcription	Rectal Smooth Muscle	rectum
47	chr5:95214400-95251800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr5:95214600-95222000	Weak transcription	Left Ventricle	heart
49	chr5:95214600-95225000	Weak transcription	Duodenum Mucosa	Duodenum
50	chr5:95214600-95230400	Weak transcription	H1 Cell Line	embryonic stem cell

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