Variant report

Variant	rs10003773
Chromosome Location	chr4:128362967-128362968
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10020135	1.00[AMR][1000 genomes]
rs28508547	1.00[AMR][1000 genomes]
rs28688904	1.00[AMR][1000 genomes]
rs28726160	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879915	chr4:128167093-129150590	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv1029214	chr4:128292215-128683123	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv537247	chr4:128292215-128683123	Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv817326	chr4:128292216-128915201	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128362400-128363200	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr4:128362400-128363600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:128362400-128364000	Enhancers	Brain Germinal Matrix	brain
4	chr4:128362400-128364000	Enhancers	Fetal Brain Female	brain
5	chr4:128362600-128363200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr4:128362600-128363200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr4:128362600-128363400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr4:128362600-128363400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr4:128362600-128363600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr4:128362600-128364400	Enhancers	Fetal Brain Male	brain

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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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