Variant report

Variant	rs4869444
Chromosome Location	chr5:35954614-35954615
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11567714	1.00[GIH][hapmap]
rs1374015	1.00[ASN][1000 genomes]
rs16874301	1.00[AFR][1000 genomes]
rs16900001	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs16902660	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16902661	1.00[JPT][hapmap];1.00[LWK][hapmap]
rs16902677	0.82[JPT][hapmap];1.00[AFR][1000 genomes]
rs16902693	1.00[AFR][1000 genomes]
rs2229232	0.82[JPT][hapmap]
rs2361394	1.00[LWK][hapmap]
rs41516445	0.91[ASN][1000 genomes]
rs4869454	1.00[AFR][1000 genomes]
rs7447304	1.00[AFR][1000 genomes]
rs889317	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv471011	chr5:35861068-36003217	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv830261	chr5:35863084-36018048	Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1025695	chr5:35902486-36036934	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35952000-35957600	Strong transcription	Liver	Liver
2	chr5:35953600-35954800	Strong transcription	Fetal Intestine Small	intestine
3	chr5:35953600-35954800	Enhancers	Fetal Thymus	thymus
4	chr5:35953800-35957800	Strong transcription	Fetal Intestine Large	intestine
5	chr5:35954000-35954800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
6	chr5:35954000-35955600	Weak transcription	Psoas Muscle	Psoas
7	chr5:35954200-35954800	Enhancers	Primary T cells from cord blood	blood
8	chr5:35954200-35954800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
9	chr5:35954200-35954800	Enhancers	Dnd41	blood
10	chr5:35954200-35955000	Strong transcription	Skeletal Muscle Male	skeletal muscle
11	chr5:35954200-35957400	Strong transcription	Skeletal Muscle Female	skeletal muscle
12	chr5:35954600-35954800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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