Variant report

Variant	rs2735483
Chromosome Location	chr17:34239178-34239179
allele	A/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	chr17:34229800-34240000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr17:34230000-34245400	Weak transcription	Primary T cells from cord blood	blood
3	chr17:34234200-34240000	Weak transcription	Fetal Intestine Large	intestine
4	chr17:34234600-34240000	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr17:34234600-34244400	Weak transcription	Thymus	Thymus
6	chr17:34234600-34251200	Weak transcription	Fetal Thymus	thymus
7	chr17:34236800-34239200	Enhancers	K562	blood
8	chr17:34237000-34240200	Weak transcription	Fetal Intestine Small	intestine
9	chr17:34237800-34239600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr17:34238400-34242400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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