Variant report

Variant	rs358714
Chromosome Location	chr3:155445425-155445426
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11923772	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs184836	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2320190	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs358720	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs358722	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs358736	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs358738	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs358740	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs358741	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs358744	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs358745	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs358746	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs358748	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs396797	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs400999	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4680215	0.85[AMR][1000 genomes];0.89[EUR][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	nsv1009618	chr3:155370034-155492177	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv829763	chr3:155417552-155470079	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
3	nsv877680	chr3:155438022-155723064	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155432400-155461600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:155436600-155447000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr3:155438400-155448800	Weak transcription	Fetal Intestine Small	intestine
4	chr3:155439200-155455600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr3:155440200-155446000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:155441600-155448800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr3:155442000-155454200	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr3:155443800-155447000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr3:155444400-155445800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr3:155444400-155446000	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr3:155444400-155446000	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr3:155444400-155446000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr3:155445200-155446200	Enhancers	Placenta	Placenta

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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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