Variant report

Variant	rs9775307
Chromosome Location	chr9:92497238-92497239
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:92465800-92507200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:92491800-92506600	Enhancers	Placenta	Placenta
3	chr9:92493600-92499000	Weak transcription	Fetal Lung	lung
4	chr9:92493600-92501400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr9:92495000-92499400	Weak transcription	Fetal Intestine Large	intestine
6	chr9:92495200-92503600	Weak transcription	Spleen	Spleen
7	chr9:92495400-92500200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr9:92496400-92497600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr9:92496400-92497600	Enhancers	Lung	lung
10	chr9:92496400-92502600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr9:92496800-92499400	Weak transcription	Fetal Intestine Small	intestine
12	chr9:92496800-92499400	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr9:92497000-92502000	Weak transcription	Fetal Heart	heart
14	chr9:92497200-92499200	Weak transcription	Liver	Liver

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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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