Variant report

Variant rs35064782
Chromosome Location chr21:46674360-46674361
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46669000-46683400 Weak transcription H9 Cell Line embryonic stem cell
2 chr21:46669200-46674600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr21:46669200-46677000 Weak transcription Left Ventricle heart
4 chr21:46669200-46706600 Weak transcription Right Atrium heart
5 chr21:46670800-46676200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr21:46671200-46683000 Weak transcription H1 Cell Line embryonic stem cell
7 chr21:46673000-46674400 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
8 chr21:46673400-46674400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr21:46673400-46675200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr21:46673400-46676600 Weak transcription Placenta Amnion Placenta Amnion
11 chr21:46673400-46681600 Weak transcription HUES6 Cell Line embryonic stem cell
12 chr21:46673600-46674400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr21:46673800-46674600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr21:46673800-46676400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
15 chr21:46673800-46683400 Weak transcription HSMM muscle

Quick Search:


  
Input of quick search could be:

what's new

Quick links