Variant report

Variant	rs2702965
Chromosome Location	chr17:34243131-34243132
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:34230000-34245400	Weak transcription	Primary T cells from cord blood	blood
2	chr17:34234600-34244400	Weak transcription	Thymus	Thymus
3	chr17:34234600-34251200	Weak transcription	Fetal Thymus	thymus
4	chr17:34239400-34243400	Enhancers	Liver	Liver
5	chr17:34239600-34244200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr17:34240200-34244200	Enhancers	Fetal Intestine Small	intestine
7	chr17:34240200-34245600	Enhancers	K562	blood
8	chr17:34240600-34244000	Enhancers	Fetal Intestine Large	intestine
9	chr17:34242600-34251400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr17:34243000-34244200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr17:34243000-34249600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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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