Variant report

Variant	rs13206047
Chromosome Location	chr6:145982939-145982940
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145950800-145990600	Weak transcription	Primary B cells from cord blood	blood
2	chr6:145951000-146003000	Weak transcription	Thymus	Thymus
3	chr6:145951400-146003000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:145952200-145983200	Weak transcription	Primary T cells from cord blood	blood
5	chr6:145973600-145990600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:145974200-146002800	Weak transcription	Liver	Liver
7	chr6:145974800-146003600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr6:145976000-145984400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr6:145976600-145984200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr6:145979400-145983800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr6:145980600-146010800	Weak transcription	Right Ventricle	heart
12	chr6:145982000-145983200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr6:145982000-145983200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr6:145982400-145983000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr6:145982400-145983400	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr6:145982600-145983400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr6:145982800-145989800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:145982800-146003000	Weak transcription	Primary B cells from peripheral blood	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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