Variant report

Variant rs4873662
Chromosome Location chr8:53474354-53474355
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:53467600-53475000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr8:53472000-53474400 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr8:53472000-53474800 Weak transcription H9 Cell Line embryonic stem cell
4 chr8:53472200-53474600 Weak transcription iPS-20b Cell Line embryonic stem cell
5 chr8:53472400-53475200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr8:53473800-53475000 Flanking Active TSS IMR90 fetal lung fibroblasts Cell Line lung
7 chr8:53474000-53474400 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr8:53474000-53474600 Enhancers H1 Cell Line embryonic stem cell
9 chr8:53474200-53474400 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
10 chr8:53474200-53474400 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr8:53474200-53474800 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
12 chr8:53474200-53474800 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
13 chr8:53474200-53475200 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
14 chr8:53474200-53475200 Bivalent Enhancer HUES6 Cell Line embryonic stem cell

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