Variant report

Variant	rs17510561
Chromosome Location	chr5:35366711-35366712
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35363600-35367800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr5:35363800-35367800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:35364800-35371800	Weak transcription	Placenta	Placenta
4	chr5:35366000-35366800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr5:35366200-35366800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr5:35366200-35367800	Enhancers	Placenta Amnion	Placenta Amnion
7	chr5:35366400-35370200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr5:35366600-35367200	Bivalent Enhancer	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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