Variant report

Variant	rs73496995
Chromosome Location	chr11:33974657-33974658
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33974000-33976600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr11:33974200-33975000	Flanking Active TSS	K562	blood
3	chr11:33974200-33975200	Enhancers	Primary hematopoietic stem cells	blood
4	chr11:33974200-33975200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr11:33974200-33975600	Enhancers	HUVEC	blood vessel
6	chr11:33974200-33975800	Enhancers	Hela-S3	cervix
7	chr11:33974400-33974800	Enhancers	H9 Cell Line	embryonic stem cell
8	chr11:33974400-33974800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr11:33974400-33975000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr11:33974400-33975000	Enhancers	HMEC	breast
11	chr11:33974400-33975200	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr11:33974400-33975200	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr11:33974400-33975200	Enhancers	NHEK	skin
14	chr11:33974600-33975000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr11:33974600-33975200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr11:33974600-33977400	Weak transcription	Primary neutrophils fromperipheralblood	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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