Variant report

Variant	rs309801
Chromosome Location	chr5:94318833-94318834
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94301200-94337600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:94312200-94323000	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr5:94313800-94337000	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr5:94314000-94323200	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr5:94314000-94325400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr5:94314800-94323000	Weak transcription	Primary hematopoietic stem cells	blood
7	chr5:94316000-94319200	Enhancers	Muscle Satellite Cultured Cells	--
8	chr5:94317600-94319400	Weak transcription	HUVEC	blood vessel
9	chr5:94318400-94321800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:94318600-94320400	Enhancers	HSMM	muscle
11	chr5:94318800-94319600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:94318800-94319800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr5:94318800-94320200	Enhancers	NHDF-Ad	bronchial
14	chr5:94318800-94321200	Enhancers	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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