Variant report

Variant	rs4106195
Chromosome Location	chr5:41528072-41528073
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41526200-41528400	Enhancers	Placenta	Placenta
2	chr5:41526400-41528400	Enhancers	HSMMtube	muscle
3	chr5:41526600-41528200	Enhancers	Muscle Satellite Cultured Cells	--
4	chr5:41526800-41528200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:41526800-41528200	Enhancers	Osteobl	bone
6	chr5:41527600-41528200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:41527800-41528200	Enhancers	Fetal Heart	heart
8	chr5:41527800-41528200	Enhancers	HSMM	muscle
9	chr5:41527800-41529200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:41528000-41528200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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