Variant report

Variant	rs2735480
Chromosome Location	chr17:34242197-34242198
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 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	chr17:34238400-34242400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr17:34239400-34243400	Enhancers	Liver	Liver
6	chr17:34239600-34244200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr17:34239800-34242600	Enhancers	HepG2	liver
8	chr17:34240200-34244200	Enhancers	Fetal Intestine Small	intestine
9	chr17:34240200-34245600	Enhancers	K562	blood
10	chr17:34240600-34244000	Enhancers	Fetal Intestine Large	intestine
11	chr17:34241200-34242400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr17:34241800-34243000	Enhancers	Placenta	Placenta

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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