Variant report

Variant	rs73088066
Chromosome Location	chr1:213501751-213501752
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213498400-213504600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr1:213498800-213501800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr1:213499200-213504200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:213500200-213504000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr1:213500400-213504600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr1:213500800-213502400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr1:213501000-213501800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:213501400-213501800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:213501400-213502600	Weak transcription	Brain Germinal Matrix	brain
10	chr1:213501400-213503600	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr1:213501400-213503600	Weak transcription	Monocytes-CD14+_RO01746	blood

Quick Search:

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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