Variant report

Variant	rs4902782
Chromosome Location	chr14:70608928-70608929
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:70606922..70609829-chr14:70609992..70611511,2	K562	blood:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1122706	0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12437377	0.82[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs12587012	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17107826	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17107875	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17107916	1.00[CHB][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs2031855	0.81[ASN][1000 genomes]
rs2840250	0.82[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs4902779	0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs4902780	0.82[JPT][hapmap]
rs4902781	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57605884	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs59651605	0.86[ASN][1000 genomes]
rs7142779	0.90[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs7157278	0.86[ASN][1000 genomes]
rs7158942	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs72476792	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs8006988	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8007664	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs8019271	0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs8020693	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs8022074	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][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	nsv832826	chr14:70559589-70723464	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70603000-70615400	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr14:70603200-70615000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr14:70603600-70615400	Weak transcription	Psoas Muscle	Psoas
4	chr14:70604000-70638000	Weak transcription	HSMMtube	muscle
5	chr14:70605400-70615400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr14:70608600-70614600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr14:70608600-70615000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr14:70608800-70609800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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