Variant report

Variant rs2839668
Chromosome Location chr10:26503114-26503115
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:26501000-26503800 Weak transcription Gastric stomach
2 chr10:26501400-26503200 Flanking Active TSS Brain Germinal Matrix brain
3 chr10:26502000-26504200 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr10:26502600-26503400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
5 chr10:26502600-26505000 Flanking Bivalent TSS/Enh iPS-18 Cell Line embryonic stem cell
6 chr10:26502600-26505200 Bivalent/Poised TSS ES-WA7 Cell Line embryonic stem cell
7 chr10:26502800-26503600 Bivalent Enhancer Dnd41 blood
8 chr10:26502800-26508600 Active TSS Pancreatic Islets Pancreatic Islet
9 chr10:26503000-26503400 Bivalent/Poised TSS H1 Cell Line embryonic stem cell
10 chr10:26503000-26503400 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
11 chr10:26503000-26503400 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell
12 chr10:26503000-26503400 Bivalent/Poised TSS iPS-20b Cell Line embryonic stem cell
13 chr10:26503000-26503400 Bivalent Enhancer Fetal Brain Female brain
14 chr10:26503000-26503600 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
15 chr10:26503000-26503600 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
16 chr10:26503000-26507800 Bivalent/Poised TSS ES-I3 Cell Line embryonic stem cell

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