Variant report

Variant	rs558415619
Chromosome Location	chr10:50801475-50801476
allele	-/AA
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000225830	Chromatin interaction
ENSG00000070748	Chromatin interaction
ENSG00000258838	Chromatin interaction
ENSG00000197444	Chromatin interaction
ENSG00000187714	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv534410	chr10:50317458-50826916	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	esv3346476	chr10:50610853-50987802	Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
4	esv3385048	chr10:50610942-50988537	Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
5	nsv1037405	chr10:50800817-50940545	Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv895378	chr10:50801342-50955649	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr10:50799800-50802800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:50800600-50801600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr10:50800600-50801800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr10:50800600-50801800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr10:50800800-50801600	Enhancers	NHEK	skin
6	chr10:50800800-50801800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:50800800-50801800	Enhancers	HMEC	breast
8	chr10:50800800-50803000	Enhancers	Hela-S3	cervix
9	chr10:50801000-50801600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr10:50801000-50801600	Enhancers	Muscle Satellite Cultured Cells	--
11	chr10:50801000-50801600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr10:50801200-50801600	Enhancers	Primary B cells from peripheral blood	blood
13	chr10:50801200-50801600	Enhancers	Liver	Liver
14	chr10:50801200-50801600	Enhancers	Brain Anterior Caudate	brain
15	chr10:50801200-50801600	Enhancers	K562	blood
16	chr10:50801200-50803600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr10:50801400-50801600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr10:50801400-50802800	Weak transcription	Osteobl	bone

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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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