Variant report

Variant	rs7513236
Chromosome Location	chr1:151704114-151704115
allele	A/C
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	chr1:151700800-151709800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:151701600-151707400	Weak transcription	Brain Anterior Caudate	brain
3	chr1:151702000-151707400	Weak transcription	Brain Angular Gyrus	brain
4	chr1:151702200-151709800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:151702600-151709600	Weak transcription	Right Atrium	heart
6	chr1:151702800-151707200	Weak transcription	Liver	Liver
7	chr1:151702800-151707400	Weak transcription	Pancreas	Pancrea
8	chr1:151702800-151707600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr1:151702800-151712200	Weak transcription	Stomach Mucosa	stomach
10	chr1:151703000-151707400	Weak transcription	Fetal Intestine Small	intestine
11	chr1:151704000-151704200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:151704000-151704400	Enhancers	HepG2	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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