Variant report

Variant	rs11776624
Chromosome Location	chr8:129951480-129951481
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129937400-129958800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:129947400-129951800	Strong transcription	Dnd41	blood
3	chr8:129947400-129952600	Enhancers	HSMM	muscle
4	chr8:129948800-129951800	Weak transcription	NHDF-Ad	bronchial
5	chr8:129949800-129952600	Enhancers	HSMMtube	muscle
6	chr8:129950400-129951600	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr8:129950400-129952200	Enhancers	Fetal Muscle Leg	muscle
8	chr8:129950600-129951800	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr8:129950800-129951600	Weak transcription	Fetal Muscle Trunk	muscle
10	chr8:129950800-129952000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr8:129951400-129951600	Enhancers	Psoas Muscle	Psoas
12	chr8:129951400-129952400	Enhancers	Fetal Stomach	stomach
13	chr8:129951400-129952600	Enhancers	Muscle Satellite Cultured Cells	--

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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