Variant report

Variant	rs72864858
Chromosome Location	chr2:37582468-37582469
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	chr2:37579913..37583058-chr2:37585203..37589963,5	K562	blood:

Variant related genes	Relation type
ENSG00000115828	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11902200	1.00[EUR][1000 genomes]
rs17020573	1.00[EUR][1000 genomes]
rs2058718	1.00[EUR][1000 genomes]
rs6722596	1.00[EUR][1000 genomes]
rs6756313	1.00[EUR][1000 genomes]
rs72864856	1.00[EUR][1000 genomes]
rs72864863	1.00[EUR][1000 genomes]
rs72864877	1.00[EUR][1000 genomes]
rs72864880	1.00[EUR][1000 genomes]
rs72864889	1.00[EUR][1000 genomes]
rs73924611	1.00[EUR][1000 genomes]
rs7564929	1.00[EUR][1000 genomes]
rs7584351	1.00[EUR][1000 genomes]
rs7596533	1.00[EUR][1000 genomes]
rs7603787	1.00[EUR][1000 genomes]
rs7606760	1.00[EUR][1000 genomes]
rs7606958	1.00[EUR][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	nsv430724	chr2:37546820-37628704	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	n/a
2	nsv2685	chr2:37550096-37594923	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37572600-37595400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:37577000-37590600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:37577400-37607000	Weak transcription	Spleen	Spleen
4	chr2:37577600-37588600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:37577800-37583200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr2:37577800-37583200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr2:37577800-37589000	Weak transcription	Left Ventricle	heart
8	chr2:37578200-37605400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr2:37578400-37604200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:37578600-37584600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr2:37578600-37584600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr2:37578600-37601200	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr2:37578800-37602200	Weak transcription	Colon Smooth Muscle	Colon
14	chr2:37579400-37584200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:37579800-37592600	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr2:37579800-37603000	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr2:37580200-37603400	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr2:37581600-37584400	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr2:37581600-37595600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr2:37581800-37588400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links