Variant report

Variant	rs17103906
Chromosome Location	chr12:67904963-67904964
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	chr12:67903000-67910600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr12:67903200-67911000	Weak transcription	Right Atrium	heart
3	chr12:67904200-67906800	Weak transcription	Fetal Heart	heart
4	chr12:67904600-67905000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr12:67904600-67905400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr12:67904600-67905400	Weak transcription	Aorta	Aorta
7	chr12:67904600-67908600	Weak transcription	Fetal Lung	lung
8	chr12:67904600-67908800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr12:67904800-67905200	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr12:67904800-67908800	Weak transcription	Pancreas	Pancrea
11	chr12:67904800-67909000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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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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