Variant report

Variant	rs568327844
Chromosome Location	chr10:52856123-52856124
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831873	chr10:52710610-52899540	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv895394	chr10:52793177-52866503	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1036645	chr10:52804961-53159076	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
4	nsv825378	chr10:52855771-52908439	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52843600-52856200	Weak transcription	Aorta	Aorta
2	chr10:52844000-52877200	Weak transcription	Fetal Stomach	stomach
3	chr10:52850200-52863400	Weak transcription	NHLF	lung
4	chr10:52852400-52856800	Weak transcription	Ovary	ovary
5	chr10:52853000-52871200	Weak transcription	Fetal Muscle Leg	muscle
6	chr10:52853200-52857600	Enhancers	Rectal Smooth Muscle	rectum
7	chr10:52853200-52860000	Weak transcription	Fetal Lung	lung
8	chr10:52853400-52856200	Weak transcription	Stomach Smooth Muscle	stomach
9	chr10:52853400-52857200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr10:52853400-52857400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr10:52853800-52856800	Weak transcription	Left Ventricle	heart
12	chr10:52853800-52858200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr10:52855200-52866200	Weak transcription	Psoas Muscle	Psoas
14	chr10:52855600-52856800	Enhancers	Fetal Heart	heart
15	chr10:52856000-52856400	Enhancers	Duodenum Smooth Muscle	Duodenum
16	chr10:52856000-52856400	Enhancers	Right Atrium	heart
17	chr10:52856000-52856600	Enhancers	Colon Smooth Muscle	Colon
18	chr10:52856000-52859200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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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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