Variant report

Variant	rs10133184
Chromosome Location	chr14:32796591-32796592
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32788800-32811800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr14:32790800-32799800	Weak transcription	Fetal Heart	heart
3	chr14:32793600-32797000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr14:32794200-32797000	Weak transcription	Brain Hippocampus Middle	brain
5	chr14:32794400-32797000	Weak transcription	Brain Substantia Nigra	brain
6	chr14:32794600-32796800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr14:32794600-32797000	Weak transcription	Brain Anterior Caudate	brain
8	chr14:32795000-32796600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr14:32796400-32797800	Enhancers	HSMMtube	muscle
10	chr14:32796400-32798000	Enhancers	K562	blood

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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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