Variant report

Variant rs116441614
Chromosome Location chr4:147554339-147554340
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:147554000-147554400 Flanking Bivalent TSS/Enh iPS-18 Cell Line embryonic stem cell
2 chr4:147554000-147554400 Bivalent/Poised TSS iPS-20b Cell Line embryonic stem cell
3 chr4:147554000-147554600 Flanking Bivalent TSS/Enh ES-UCSF4 Cell Line embryonic stem cell
4 chr4:147554000-147554600 Bivalent Enhancer Fetal Brain Male brain
5 chr4:147554000-147555000 Flanking Bivalent TSS/Enh iPS-15b Cell Line embryonic stem cell
6 chr4:147554000-147555200 Bivalent/Poised TSS H9 Cell Line embryonic stem cell
7 chr4:147554200-147554400 Bivalent/Poised TSS ES-I3 Cell Line embryonic stem cell
8 chr4:147554200-147554400 Bivalent Enhancer H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr4:147554200-147554400 Flanking Bivalent TSS/Enh HUES64 Cell Line embryonic stem cell
10 chr4:147554200-147554400 Flanking Bivalent TSS/Enh iPS DF 6.9 Cell Line embryonic stem cell
11 chr4:147554200-147554400 Flanking Bivalent TSS/Enh iPS DF 19.11 Cell Line embryonic stem cell
12 chr4:147554200-147554400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
13 chr4:147554200-147554400 Bivalent Enhancer Fetal Brain Female brain
14 chr4:147554200-147554600 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr4:147554200-147554600 Bivalent Enhancer Fetal Heart heart
16 chr4:147554200-147554800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
17 chr4:147554200-147555000 Flanking Bivalent TSS/Enh H1 Cell Line embryonic stem cell
18 chr4:147554200-147555000 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
19 chr4:147554200-147555000 Bivalent Enhancer Brain Hippocampus Middle brain
20 chr4:147554200-147555200 Bivalent Enhancer Cortex derived primary cultured neurospheres brain

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