Variant report

Variant	rs11181819
Chromosome Location	chr12:43353547-43353548
allele	A/T
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	chr12:43350000-43353600	Enhancers	Fetal Brain Male	brain
2	chr12:43350800-43356200	Weak transcription	Fetal Lung	lung
3	chr12:43351400-43357000	Enhancers	HMEC	breast
4	chr12:43351400-43357800	Enhancers	Muscle Satellite Cultured Cells	--
5	chr12:43351400-43357800	Enhancers	HUVEC	blood vessel
6	chr12:43351600-43357000	Enhancers	NHEK	skin
7	chr12:43351800-43356800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr12:43351800-43359600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr12:43352200-43355000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:43352600-43353600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:43352800-43354600	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr12:43353000-43355200	Weak transcription	Fetal Muscle Leg	muscle
13	chr12:43353000-43355600	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr12:43353200-43357000	Enhancers	Hela-S3	cervix

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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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