Variant report

Variant rs56275097
Chromosome Location chr8:104962726-104962727
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:104948200-104965200 Weak transcription Brain Inferior Temporal Lobe brain
2 chr8:104951800-104964000 Weak transcription iPS-15b Cell Line embryonic stem cell
3 chr8:104952000-104977000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr8:104955600-104969600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr8:104959800-104963600 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr8:104960000-104963000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr8:104960400-104962800 Weak transcription iPS-20b Cell Line embryonic stem cell
8 chr8:104960400-104975800 Weak transcription H1 Cell Line embryonic stem cell
9 chr8:104960600-104964000 Weak transcription HUES64 Cell Line embryonic stem cell
10 chr8:104960800-104967000 Weak transcription Fetal Adrenal Gland Adrenal Gland
11 chr8:104960800-104975600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr8:104961000-104976000 Weak transcription HUES48 Cell Line embryonic stem cell
13 chr8:104962600-104964400 ZNF genes & repeats H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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