Variant report

Variant	rs7588455
Chromosome Location	chr2:55087107-55087108
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	chr2:55085400..55087533-chr2:55090149..55092630,2	MCF-7	breast:
2	chr2:55087086..55089357-chr2:55090408..55092933,2	K562	blood:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12713280	0.82[ASN][1000 genomes]
rs12713281	0.92[ASN][1000 genomes]
rs12713283	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1347816	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35459932	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4613325	0.87[ASN][1000 genomes]
rs6545451	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs67025912	0.97[ASN][1000 genomes]
rs6756000	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7559919	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33638	chr2:54765256-55109455	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv1005449	chr2:54938633-55129503	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv457930	chr2:55073428-55091029	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv582028	chr2:55073428-55091029	Enhancers Flanking Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv1796192	chr2:55081033-55110969	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55066800-55088800	Weak transcription	Brain Substantia Nigra	brain
2	chr2:55068400-55096200	Weak transcription	Brain Cingulate Gyrus	brain
3	chr2:55068400-55109000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr2:55068600-55122400	Weak transcription	Brain Anterior Caudate	brain
5	chr2:55072600-55091600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr2:55073400-55093800	Weak transcription	Primary B cells from peripheral blood	blood
7	chr2:55078000-55087600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:55078800-55106800	Weak transcription	Brain Angular Gyrus	brain
9	chr2:55081400-55122400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr2:55084400-55088800	Enhancers	HSMMtube	muscle
11	chr2:55084800-55088400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr2:55084800-55088400	Enhancers	Fetal Muscle Leg	muscle
13	chr2:55085400-55088200	Enhancers	NHDF-Ad	bronchial
14	chr2:55085800-55087200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr2:55086000-55087400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr2:55086000-55087400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr2:55086000-55088600	Enhancers	HSMM	muscle
18	chr2:55086200-55087200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr2:55086400-55090400	Weak transcription	Liver	Liver
20	chr2:55086600-55088000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr2:55087000-55087400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
22	chr2:55087000-55087400	Flanking Active TSS	NH-A	brain
23	chr2:55087000-55087800	Enhancers	Placenta	Placenta
24	chr2:55087000-55088000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:55087000-55088000	Enhancers	Psoas Muscle	Psoas
26	chr2:55087000-55088200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr2:55087000-55088200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr2:55087000-55088200	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr2:55087000-55088200	Enhancers	NHEK	skin
30	chr2:55087000-55088400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr2:55087000-55088400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr2:55087000-55088400	Enhancers	Osteobl	bone
33	chr2:55087000-55088600	Enhancers	Muscle Satellite Cultured Cells	--
34	chr2:55087000-55098600	Weak transcription	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links