Variant report

Variant	rs4902775
Chromosome Location	chr14:70545938-70545939
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1009256	0.99[ASN][1000 genomes]
rs10873226	0.97[ASN][1000 genomes]
rs11158830	0.99[ASN][1000 genomes]
rs11850085	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12586172	0.97[ASN][1000 genomes]
rs12589441	0.95[ASN][1000 genomes]
rs12590573	0.97[ASN][1000 genomes]
rs12883784	0.97[ASN][1000 genomes]
rs12883875	0.97[ASN][1000 genomes]
rs12884186	0.97[ASN][1000 genomes]
rs12888543	0.97[ASN][1000 genomes]
rs12889279	0.99[ASN][1000 genomes]
rs12890130	0.96[ASN][1000 genomes]
rs1364967	0.84[ASN][1000 genomes]
rs1459707	0.90[ASN][1000 genomes]
rs149250	0.89[ASN][1000 genomes]
rs149595	0.92[ASN][1000 genomes]
rs150942	0.97[ASN][1000 genomes]
rs150946	0.92[ASN][1000 genomes]
rs150954	0.89[ASN][1000 genomes]
rs150955	0.87[ASN][1000 genomes]
rs150956	0.89[ASN][1000 genomes]
rs17107768	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs178921	0.97[ASN][1000 genomes]
rs178923	0.88[ASN][1000 genomes]
rs1958184	0.97[ASN][1000 genomes]
rs2169074	0.97[ASN][1000 genomes]
rs4144997	0.99[ASN][1000 genomes]
rs4899324	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4899325	0.88[ASN][1000 genomes]
rs4902772	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4902776	0.99[ASN][1000 genomes]
rs57170277	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs57898302	0.88[ASN][1000 genomes]
rs6573922	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6573924	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7148389	0.86[ASN][1000 genomes]
rs7161555	0.99[ASN][1000 genomes]
rs8006790	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8006924	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8013012	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs8015112	0.88[ASN][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	nsv456336	chr14:70081956-70574149	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv565007	chr14:70081956-70574149	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70526400-70549000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:70530600-70548800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:70536800-70552200	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr14:70539000-70552200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr14:70545000-70547800	Enhancers	Fetal Brain Male	brain
6	chr14:70545400-70546400	Weak transcription	Pancreas	Pancrea

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