Variant report

Variant	rs10217025
Chromosome Location	chr8:102804307-102804308
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:102803200-102804400	Enhancers	Stomach Mucosa	stomach
2	chr8:102803200-102805000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:102803200-102805000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr8:102803200-102817800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:102803400-102805000	Enhancers	Psoas Muscle	Psoas
6	chr8:102803600-102870600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr8:102803800-102805000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:102803800-102805200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr8:102803800-102805400	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr8:102804000-102804800	Enhancers	Fetal Brain Female	brain
11	chr8:102804000-102805000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr8:102804000-102805000	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr8:102804200-102804600	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr8:102804200-102804600	Weak transcription	GM12878-XiMat	blood
15	chr8:102804200-102806000	Weak transcription	Ovary	ovary
16	chr8:102804200-102807400	Weak transcription	Fetal Brain Male	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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