Variant report

Variant	rs16866933
Chromosome Location	chr2:180566678-180566679
allele	A/G
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	chr2:180540400-180571200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:180566200-180566800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:180566400-180566800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:180566400-180566800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr2:180566400-180566800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:180566400-180566800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr2:180566400-180566800	Flanking Active TSS	HSMM	muscle
8	chr2:180566400-180566800	Enhancers	HSMMtube	muscle
9	chr2:180566400-180566800	Enhancers	NHEK	skin
10	chr2:180566400-180566800	Enhancers	Osteobl	bone
11	chr2:180566400-180568400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:180566600-180566800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:180566600-180568200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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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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