Variant report

Variant	rs68134266
Chromosome Location	chr4:160528014-160528015
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11933100	0.91[ASN][1000 genomes]
rs13112156	0.93[ASN][1000 genomes]
rs13112713	0.89[ASN][1000 genomes]
rs13149175	0.95[ASN][1000 genomes]
rs35952229	0.91[ASN][1000 genomes]
rs4516668	0.89[ASN][1000 genomes]
rs56121133	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs59810355	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs61089717	0.82[ASN][1000 genomes]
rs62337313	0.82[ASN][1000 genomes]
rs62337315	0.82[ASN][1000 genomes]
rs7683151	0.93[ASN][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	nsv1015469	chr4:160389277-160841619	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537316	chr4:160389277-160841619	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv881205	chr4:160516090-160628006	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160516800-160530000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:160519600-160528200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr4:160524600-160528400	Weak transcription	Fetal Intestine Large	intestine
4	chr4:160524600-160528600	Weak transcription	Pancreas	Pancrea
5	chr4:160526800-160530400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:160527000-160528800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
7	chr4:160527200-160528400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr4:160527400-160536400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:160527600-160528600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
10	chr4:160527800-160530000	Enhancers	HMEC	breast
11	chr4:160528000-160528200	Weak transcription	H1 Derived Neuronal Progenitor Cultured 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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