Variant report

Variant	rs6670596
Chromosome Location	chr1:57282068-57282069
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11579186	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6662900	0.94[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6672416	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6672492	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6682939	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72668402	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7547964	0.83[CEU][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869295	chr1:56894955-57656562	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57277400-57282600	Weak transcription	HMEC	breast
2	chr1:57278400-57283000	Weak transcription	Fetal Heart	heart
3	chr1:57278800-57283000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr1:57278800-57284400	Weak transcription	Right Ventricle	heart
5	chr1:57279000-57283400	Weak transcription	Fetal Kidney	kidney
6	chr1:57280000-57282800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:57280000-57283400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr1:57280000-57283800	Weak transcription	Gastric	stomach
9	chr1:57280200-57283400	Weak transcription	Esophagus	oesophagus
10	chr1:57280400-57285000	Weak transcription	Lung	lung
11	chr1:57280800-57284200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:57281200-57282600	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr1:57281400-57283000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:57281400-57283400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:57281400-57284000	Enhancers	Fetal Intestine Large	intestine
16	chr1:57281400-57284600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr1:57281800-57282600	Flanking Active TSS	Liver	Liver
18	chr1:57281800-57283600	Weak transcription	Osteobl	bone
19	chr1:57281800-57287600	Enhancers	Fetal Intestine Small	intestine
20	chr1:57282000-57282200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:57282000-57282400	Weak transcription	Psoas Muscle	Psoas
22	chr1:57282000-57282800	Weak transcription	Left Ventricle	heart
23	chr1:57282000-57283800	Enhancers	HepG2	liver
24	chr1:57282000-57285600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links