Variant report

Variant	rs545629363
Chromosome Location	chr4:148116578-148116579
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024629	chr4:147987351-148277008	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases
2	nsv830108	chr4:148114652-148311104	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148111800-148117800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:148115200-148117000	Enhancers	Muscle Satellite Cultured Cells	--
3	chr4:148115200-148117000	Enhancers	HSMM	muscle
4	chr4:148115400-148116600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr4:148115400-148116600	Enhancers	HSMMtube	muscle
6	chr4:148115400-148116800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr4:148115400-148116800	Enhancers	NHDF-Ad	bronchial
8	chr4:148115400-148117000	Enhancers	NH-A	brain
9	chr4:148115800-148116800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr4:148115800-148119400	Weak transcription	Fetal Heart	heart
11	chr4:148116000-148116600	Enhancers	Fetal Kidney	kidney
12	chr4:148116000-148116800	Enhancers	Ovary	ovary
13	chr4:148116200-148116600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr4:148116200-148116600	Enhancers	NHLF	lung
15	chr4:148116200-148119600	Weak transcription	Fetal Stomach	stomach
16	chr4:148116200-148120800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr4:148116400-148117000	Enhancers	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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