Variant report

Variant rs74161326
Chromosome Location chr10:118569994-118569995
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:118560600-118586200 Weak transcription H9 Cell Line embryonic stem cell
2 chr10:118563400-118575400 Weak transcription Brain Angular Gyrus brain
3 chr10:118568600-118570400 Enhancers H1 Cell Line embryonic stem cell
4 chr10:118569000-118570000 Enhancers iPS-15b Cell Line embryonic stem cell
5 chr10:118569000-118570000 Bivalent Enhancer Fetal Lung lung
6 chr10:118569000-118570000 Active TSS HMEC breast
7 chr10:118569200-118570000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr10:118569200-118570800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr10:118569400-118570000 Active TSS Pancreatic Islets Pancreatic Islet
10 chr10:118569400-118570200 Enhancers HUES48 Cell Line embryonic stem cell
11 chr10:118569400-118570200 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr10:118569400-118570400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
13 chr10:118569600-118570000 Bivalent/Poised TSS Breast Myoepithelial Primary Cells Breast
14 chr10:118569600-118570200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr10:118569600-118586200 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr10:118569600-118592600 Weak transcription Pancreas Pancrea
17 chr10:118569800-118572200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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