Variant report

Variant	rs12594562
Chromosome Location	chr15:49266088-49266089
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:49256400-49266800	Weak transcription	Brain Substantia Nigra	brain
2	chr15:49256400-49267200	Weak transcription	Aorta	Aorta
3	chr15:49259600-49267400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr15:49260200-49267800	Weak transcription	HSMM	muscle
5	chr15:49260800-49267200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr15:49263800-49267800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr15:49265200-49267800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr15:49265400-49267800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr15:49265600-49268000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr15:49265800-49266200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr15:49265800-49268000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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