Variant report

Variant	rs60703665
Chromosome Location	chr1:48391863-48391864
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:48384000-48392200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr1:48384200-48392400	Weak transcription	Esophagus	oesophagus
3	chr1:48384400-48392600	Weak transcription	Right Ventricle	heart
4	chr1:48384600-48392000	Weak transcription	Aorta	Aorta
5	chr1:48385600-48392000	Weak transcription	Right Atrium	heart
6	chr1:48386200-48392400	Weak transcription	Spleen	Spleen
7	chr1:48387000-48393800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr1:48388200-48399200	Weak transcription	Liver	Liver
9	chr1:48390400-48392400	Weak transcription	Fetal Muscle Leg	muscle
10	chr1:48390600-48392400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:48390600-48395600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:48390800-48392200	Weak transcription	NHEK	skin
13	chr1:48390800-48392400	Weak transcription	HepG2	liver
14	chr1:48390800-48398600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr1:48391400-48403800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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