Variant report

Variant	rs6782203
Chromosome Location	chr3:142671596-142671597
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000163714	Chromatin interaction
ENSG00000241592	Chromatin interaction
ENSG00000241570	Chromatin interaction
ENSG00000188582	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs3732742	1.00[ASN][1000 genomes]
rs6781427	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6782209	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73003356	1.00[ASN][1000 genomes]
rs73866279	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73866283	0.84[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs73866284	0.84[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7627274	1.00[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	nsv877562	chr3:142573789-142846370	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv4040	chr3:142649146-142675752	Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv877563	chr3:142661350-142743889	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142667000-142671800	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr3:142667000-142671800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:142667200-142681000	Weak transcription	Right Ventricle	heart
4	chr3:142669200-142680800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:142669600-142671600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr3:142670000-142672000	Enhancers	HepG2	liver
7	chr3:142671400-142672000	Enhancers	Right Atrium	heart
8	chr3:142671400-142672000	Flanking Active TSS	K562	blood
9	chr3:142671400-142672800	Enhancers	Liver	Liver

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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

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