Variant report

Variant	rs73955290
Chromosome Location	chr2:113600565-113600566
allele	C/G
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	chr2:113594400-113601200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr2:113596000-113600800	Enhancers	Primary B cells from peripheral blood	blood
3	chr2:113597400-113600600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr2:113598200-113600600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
5	chr2:113598200-113603400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr2:113599400-113600600	Enhancers	NHEK	skin
7	chr2:113599400-113600800	Enhancers	GM12878-XiMat	blood
8	chr2:113599600-113601000	Enhancers	Primary B cells from cord blood	blood
9	chr2:113600400-113600600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr2:113600400-113603400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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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