Variant report

Variant	rs17316198
Chromosome Location	chr1:63247772-63247773
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:63244200-63249200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr1:63244200-63249400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr1:63245800-63248400	Weak transcription	Placenta	Placenta
4	chr1:63245800-63249400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:63246000-63249200	Weak transcription	K562	blood
6	chr1:63246200-63248800	Weak transcription	A549	lung
7	chr1:63246800-63248400	Enhancers	HepG2	liver
8	chr1:63247000-63248800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr1:63247400-63248000	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr1:63247400-63248400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:63247600-63248000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:63247600-63248400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr1:63247600-63249000	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr1:63247600-63249000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr1:63247600-63249000	Enhancers	Dnd41	blood
16	chr1:63247600-63249200	Weak transcription	Fetal Brain Male	brain

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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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