Variant report

Variant	rs8005048
Chromosome Location	chr14:79189973-79189974
allele	A/G
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	chr14:79187200-79190000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr14:79187400-79190000	Enhancers	Brain Germinal Matrix	brain
3	chr14:79187600-79190000	Enhancers	Brain Hippocampus Middle	brain
4	chr14:79187600-79192400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:79188600-79190000	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr14:79188800-79191200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr14:79189200-79190000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr14:79189200-79191200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr14:79189400-79191200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr14:79189400-79198200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr14:79189600-79193600	Weak transcription	Brain Angular Gyrus	brain

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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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