Variant report

Variant	rs6797712
Chromosome Location	chr3:178689388-178689389
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11719643	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12494207	0.90[ASN][1000 genomes]
rs28709897	0.99[ASN][1000 genomes]
rs4607154	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4621371	0.96[ASN][1000 genomes]
rs4955795	0.89[EUR][1000 genomes]
rs4955798	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56182354	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61323110	0.89[ASN][1000 genomes]
rs61796632	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61798163	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6787571	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6800994	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72622562	0.96[ASN][1000 genomes]
rs7618985	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9823404	0.92[ASN][1000 genomes]
rs9836168	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9882690	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998253	chr3:178622707-179196274	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv536814	chr3:178622707-179196274	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv1010148	chr3:178650949-178691377	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv461026	chr3:178661814-178886609	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv592649	chr3:178661814-178886609	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:178683600-178691200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:178685200-178689400	Weak transcription	Hela-S3	cervix
3	chr3:178685200-178689600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:178685200-178689600	Weak transcription	Pancreas	Pancrea
5	chr3:178685200-178690000	Weak transcription	Right Atrium	heart
6	chr3:178685200-178705200	Weak transcription	HSMMtube	muscle
7	chr3:178685400-178689400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr3:178685400-178689400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr3:178685800-178689400	Weak transcription	HSMM	muscle
10	chr3:178686400-178689400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr3:178688200-178691000	Weak transcription	GM12878-XiMat	blood

Quick Search:

Input of quick search could be:

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

what's new

Quick links