Variant report

Variant	rs17106935
Chromosome Location	chr14:78602934-78602935
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78598600-78613000	Weak transcription	Brain Substantia Nigra	brain
2	chr14:78600800-78603000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr14:78601000-78603400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr14:78601400-78603000	Enhancers	Primary hematopoietic stem cells	blood
5	chr14:78601400-78603200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr14:78601600-78603000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr14:78601800-78603000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr14:78602400-78603200	Enhancers	NHEK	skin
9	chr14:78602600-78603200	Enhancers	A549	lung

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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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