Variant report

Variant	rs72672141
Chromosome Location	chr8:118558590-118558591
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118542000-118558600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr8:118546600-118558600	Weak transcription	Primary B cells from cord blood	blood
3	chr8:118546600-118559400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr8:118546600-118561600	Weak transcription	Osteobl	bone
5	chr8:118546800-118561600	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr8:118546800-118562200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:118548000-118560400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr8:118554200-118561600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr8:118555000-118561800	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr8:118558000-118564400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr8:118558400-118559000	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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