Variant report

Variant	rs12187655
Chromosome Location	chr5:36388992-36388993
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36375000-36390600	Weak transcription	Lung	lung
2	chr5:36381000-36393600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:36385200-36392200	Weak transcription	Spleen	Spleen
4	chr5:36385400-36389000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr5:36385400-36389000	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr5:36385400-36389200	Weak transcription	Primary hematopoietic stem cells	blood
7	chr5:36385800-36389000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:36387800-36389200	Enhancers	Placenta	Placenta
9	chr5:36387800-36391000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr5:36388000-36390000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:36388200-36389800	Enhancers	Fetal Kidney	kidney
12	chr5:36388600-36389800	Enhancers	Ovary	ovary
13	chr5:36388600-36391200	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr5:36388600-36391800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr5:36388800-36390000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr5:36388800-36390000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr5:36388800-36390000	Enhancers	Fetal Lung	lung
18	chr5:36388800-36391600	Enhancers	Primary hematopoietic stem cells short term culture	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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