Variant report

Variant	rs709792
Chromosome Location	chr1:85680783-85680784
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1674180	1.00[EUR][1000 genomes]
rs1870326	1.00[EUR][1000 genomes]
rs2790912	1.00[EUR][1000 genomes]
rs709784	1.00[EUR][1000 genomes]
rs709791	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs817408	1.00[EUR][1000 genomes]
rs817412	1.00[EUR][1000 genomes]
rs817442	1.00[EUR][1000 genomes]
rs817443	1.00[EUR][1000 genomes]
rs817444	1.00[EUR][1000 genomes]
rs817448	1.00[EUR][1000 genomes]
rs817450	1.00[EUR][1000 genomes]
rs971243	1.00[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	nsv1006994	chr1:85454304-86327679	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	esv34165	chr1:85542040-85846249	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv830459	chr1:85589585-85786311	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 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	chr1:85668000-85689000	Weak transcription	Gastric	stomach
2	chr1:85668600-85680800	Weak transcription	K562	blood
3	chr1:85673200-85681200	Weak transcription	Colon Smooth Muscle	Colon
4	chr1:85673800-85690400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr1:85679800-85682000	Enhancers	HepG2	liver
6	chr1:85680000-85681400	Enhancers	Stomach Mucosa	stomach
7	chr1:85680000-85681400	Enhancers	A549	lung
8	chr1:85680200-85681000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:85680400-85681000	Flanking Active TSS	Hela-S3	cervix
10	chr1:85680600-85680800	Active TSS	Stomach Smooth Muscle	stomach
11	chr1:85680600-85681000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr1:85680600-85681200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:85680600-85681200	Weak transcription	Rectal Smooth Muscle	rectum

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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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