Variant report

Variant	rs72972224
Chromosome Location	chr3:133388261-133388262
allele	A/G
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	chr3:133381400-133392400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:133381600-133388800	Weak transcription	Gastric	stomach
3	chr3:133382800-133388400	Enhancers	HepG2	liver
4	chr3:133382800-133390200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:133382800-133392800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr3:133383000-133389000	Weak transcription	Fetal Intestine Small	intestine
7	chr3:133383000-133389000	Weak transcription	A549	lung
8	chr3:133386400-133389600	Enhancers	Liver	Liver
9	chr3:133387200-133390000	Enhancers	Pancreas	Pancrea
10	chr3:133387600-133389800	Enhancers	Fetal Intestine Large	intestine
11	chr3:133387800-133389400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr3:133387800-133393000	Weak transcription	Right Atrium	heart

Quick Search:

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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