Variant report

Variant rs6848399
Chromosome Location chr4:118823657-118823658
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:118821200-118823800 Enhancers Primary neutrophils fromperipheralblood blood
2 chr4:118821200-118824400 Enhancers HUES48 Cell Line embryonic stem cell
3 chr4:118821600-118824200 Weak transcription H9 Cell Line embryonic stem cell
4 chr4:118822400-118823800 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr4:118822400-118824000 Weak transcription H1 Cell Line embryonic stem cell
6 chr4:118822600-118826600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr4:118822800-118824200 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr4:118823000-118824000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
9 chr4:118823000-118824000 Weak transcription HUES6 Cell Line embryonic stem cell
10 chr4:118823000-118824000 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chr4:118823200-118823800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr4:118823200-118826200 Weak transcription Stomach Mucosa stomach
13 chr4:118823600-118824200 Bivalent Enhancer hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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