Variant report

Variant	rs10136775
Chromosome Location	chr14:32790813-32790814
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32777400-32791400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:32788600-32791400	Weak transcription	Esophagus	oesophagus
3	chr14:32788800-32811800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr14:32789400-32791000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr14:32790600-32791400	Enhancers	NHEK	skin
6	chr14:32790800-32791200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr14:32790800-32791400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr14:32790800-32799800	Weak transcription	Fetal Heart	heart

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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