Variant report

Variant	rs11848201
Chromosome Location	chr14:69080859-69080860
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69075200-69081200	Weak transcription	Fetal Brain Male	brain
2	chr14:69079200-69081000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr14:69079200-69085400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr14:69079400-69083200	Weak transcription	Fetal Heart	heart
5	chr14:69080400-69081000	ZNF genes & repeats	Liver	Liver
6	chr14:69080400-69084600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr14:69080600-69081000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
8	chr14:69080600-69081000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
9	chr14:69080800-69081600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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