Variant report

Variant	rs1354440
Chromosome Location	chr3:68811959-68811960
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11706249	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11708245	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11717220	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13320444	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13321204	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1387729	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1387730	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1387732	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1387733	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1504295	0.84[AFR][1000 genomes]
rs1602197	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1602198	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1602201	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2130437	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28475377	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2872443	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs28758872	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4632549	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs56174174	0.82[AMR][1000 genomes]
rs62254083	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62254085	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62254087	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62254089	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62254091	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7629966	0.80[EUR][1000 genomes]
rs7648643	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9310132	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs971381	0.82[AFR][1000 genomes]
rs9756913	0.80[EUR][1000 genomes]
rs9817600	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9822359	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9824091	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9835691	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9840400	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9850052	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9851134	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9851941	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9866307	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9867467	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9882142	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]

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	nsv834722	chr3:68775036-68974120	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:68808400-68813200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:68808800-68813200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr3:68809200-68813200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr3:68809200-68813600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr3:68810200-68813200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:68810200-68824400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr3:68810800-68813200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr3:68811000-68813200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr3:68811000-68813200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr3:68811000-68813600	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr3:68811200-68813200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links