Variant report

Variant	rs1520826
Chromosome Location	chr12:43353711-43353712
allele	G/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	chr12:43350800-43356200	Weak transcription	Fetal Lung	lung
2	chr12:43351400-43357000	Enhancers	HMEC	breast
3	chr12:43351400-43357800	Enhancers	Muscle Satellite Cultured Cells	--
4	chr12:43351400-43357800	Enhancers	HUVEC	blood vessel
5	chr12:43351600-43357000	Enhancers	NHEK	skin
6	chr12:43351800-43356800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr12:43351800-43359600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr12:43352200-43355000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr12:43352800-43354600	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr12:43353000-43355200	Weak transcription	Fetal Muscle Leg	muscle
11	chr12:43353000-43355600	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr12:43353200-43357000	Enhancers	Hela-S3	cervix
13	chr12:43353600-43354000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr12:43353600-43354600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr12:43353600-43356600	Enhancers	NH-A	brain

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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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