Variant report

Variant	rs11899742
Chromosome Location	chr2:114569651-114569652
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114565000-114569800	Weak transcription	A549	lung
2	chr2:114567400-114576000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr2:114568200-114586000	Weak transcription	Primary T cells from cord blood	blood
4	chr2:114568400-114570200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:114568600-114570600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr2:114569400-114570000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:114569400-114570200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:114569400-114570200	Enhancers	NHDF-Ad	bronchial
9	chr2:114569600-114570000	Enhancers	Fetal Heart	heart
10	chr2:114569600-114570000	Enhancers	Right Ventricle	heart

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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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