Variant report

Variant rs543389937
Chromosome Location chr4:92190209-92190210
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:92188000-92190600 Enhancers iPS-18 Cell Line embryonic stem cell
2 chr4:92188600-92190800 Enhancers HUES64 Cell Line embryonic stem cell
3 chr4:92188600-92191000 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr4:92189000-92190400 Enhancers Stomach Mucosa stomach
5 chr4:92189000-92190600 Enhancers H1 Cell Line embryonic stem cell
6 chr4:92189200-92190400 Enhancers HUES48 Cell Line embryonic stem cell
7 chr4:92189600-92190600 Weak transcription iPS-20b Cell Line embryonic stem cell
8 chr4:92190000-92190400 Flanking Active TSS ES-I3 Cell Line embryonic stem cell
9 chr4:92190000-92190400 Flanking Active TSS HUES6 Cell Line embryonic stem cell
10 chr4:92190000-92190400 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr4:92190200-92190600 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr4:92190200-92190600 Flanking Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr4:92190200-92190600 Enhancers Fetal Intestine Large intestine
14 chr4:92190200-92191000 Enhancers ES-WA7 Cell Line embryonic stem cell

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