Variant report

Variant	rs73860642
Chromosome Location	chr3:100158190-100158191
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	chr3:100130600-100162800	Weak transcription	Fetal Brain Male	brain
2	chr3:100144200-100175600	Weak transcription	Psoas Muscle	Psoas
3	chr3:100145200-100162400	Weak transcription	HepG2	liver
4	chr3:100146400-100163200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr3:100146400-100177800	Weak transcription	Ovary	ovary
6	chr3:100148200-100182400	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr3:100149400-100162400	Weak transcription	Fetal Lung	lung
8	chr3:100149400-100171800	Weak transcription	Aorta	Aorta
9	chr3:100155000-100160000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr3:100156200-100158600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr3:100157000-100158400	Enhancers	Fetal Intestine Large	intestine
12	chr3:100157400-100158600	Enhancers	Pancreas	Pancrea
13	chr3:100157600-100158800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:100157800-100160000	Weak transcription	Osteobl	bone
15	chr3:100158000-100159000	Weak transcription	H1 BMP4 Derived Mesendoderm 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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