Variant report

Variant	rs16922873
Chromosome Location	chr10:23272971-23272972
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23265000-23277600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr10:23268000-23274200	Weak transcription	Brain Hippocampus Middle	brain
3	chr10:23268200-23277800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr10:23270600-23276000	Weak transcription	Brain Angular Gyrus	brain
5	chr10:23270600-23277600	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr10:23270800-23274400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr10:23271400-23273200	Enhancers	Brain Cingulate Gyrus	brain
8	chr10:23272400-23273200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr10:23272400-23275600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr10:23272600-23273000	Enhancers	Primary hematopoietic stem cells	blood
11	chr10:23272600-23273200	Enhancers	Brain Substantia Nigra	brain
12	chr10:23272600-23273400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr10:23272800-23273000	Enhancers	Brain Anterior Caudate	brain

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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