Variant report

Variant	rs10401148
Chromosome Location	chr19:39479443-39479444
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39478800-39480800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr19:39479000-39479600	Weak transcription	Adipose Nuclei	Adipose
3	chr19:39479000-39483200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr19:39479400-39479600	Enhancers	A549	lung
5	chr19:39479400-39479600	Enhancers	HSMMtube	muscle
6	chr19:39479400-39479800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr19:39479400-39479800	Enhancers	Fetal Muscle Trunk	muscle
8	chr19:39479400-39480000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr19:39479400-39480000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr19:39479400-39480200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr19:39479400-39480800	Enhancers	HepG2	liver
12	chr19:39479400-39481000	Enhancers	Fetal Heart	heart

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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