Variant report

Variant	rs9324141
Chromosome Location	chr1:85285373-85285374
allele	C/T
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	chr1:85264000-85295600	Weak transcription	NHEK	skin
2	chr1:85266400-85287200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr1:85277000-85285400	Weak transcription	Left Ventricle	heart
4	chr1:85278200-85287200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:85281200-85289200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:85282400-85295800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:85284400-85286000	Enhancers	Primary T cells from cord blood	blood
8	chr1:85284600-85285400	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr1:85284600-85285800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr1:85284800-85287800	Enhancers	Fetal Heart	heart

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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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