Variant report

Variant	rs58801062
Chromosome Location	chr1:211884436-211884437
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211879200-211884600	Weak transcription	Esophagus	oesophagus
2	chr1:211879200-211913600	Weak transcription	Right Atrium	heart
3	chr1:211880200-211884600	Weak transcription	NHEK	skin
4	chr1:211880400-211884600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:211883600-211885200	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr1:211883800-211884600	Enhancers	HepG2	liver
7	chr1:211883800-211885200	Enhancers	K562	blood
8	chr1:211884000-211885000	Enhancers	Spleen	Spleen
9	chr1:211884200-211884600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr1:211884200-211884800	Enhancers	Primary B cells from peripheral blood	blood
11	chr1:211884200-211885000	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr1:211884200-211885000	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr1:211884200-211885000	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr1:211884200-211885400	Enhancers	Foreskin Melanocyte 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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