Variant report

Variant	rs73682910
Chromosome Location	chr7:15788271-15788272
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10234886	0.84[ASN][1000 genomes]
rs10238237	0.82[ASN][1000 genomes]
rs10264302	0.84[ASN][1000 genomes]
rs17169055	0.84[ASN][1000 genomes]
rs17169056	0.84[ASN][1000 genomes]
rs17169060	0.83[ASN][1000 genomes]
rs2019593	0.97[ASN][1000 genomes]
rs2098047	0.95[ASN][1000 genomes]
rs61619427	0.82[ASN][1000 genomes]
rs6954991	0.82[ASN][1000 genomes]
rs9769136	0.82[ASN][1000 genomes]
rs9769335	0.82[ASN][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	nsv932168	chr7:15573437-15895294	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv523199	chr7:15582208-16042596	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv830911	chr7:15666307-15817662	Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv428501	chr7:15666307-15817662	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv527639	chr7:15766594-15795567	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15787200-15789400	Weak transcription	Osteobl	bone
2	chr7:15787600-15789400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr7:15787800-15789800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr7:15788000-15789000	Weak transcription	Fetal Stomach	stomach
5	chr7:15788000-15789000	Weak transcription	Ovary	ovary
6	chr7:15788000-15789000	Weak transcription	NHDF-Ad	bronchial
7	chr7:15788000-15789200	Weak transcription	Fetal Lung	lung
8	chr7:15788000-15789400	Weak transcription	Colon Smooth Muscle	Colon
9	chr7:15788000-15790200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:15788000-15791200	Weak transcription	Adipose Nuclei	Adipose
11	chr7:15788000-15793400	Weak transcription	Stomach Smooth Muscle	stomach
12	chr7:15788200-15789200	Weak transcription	Fetal Heart	heart
13	chr7:15788200-15790400	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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