Variant report

Variant rs542298227
Chromosome Location chr10:22771649-22771650
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:22765800-22806600 Weak transcription Right Atrium heart
2 chr10:22770600-22771800 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
3 chr10:22771000-22771800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr10:22771000-22771800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
5 chr10:22771000-22771800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr10:22771000-22772200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr10:22771000-22772200 Enhancers GM12878-XiMat blood
8 chr10:22771000-22780200 Weak transcription Brain Angular Gyrus brain
9 chr10:22771200-22772000 Enhancers Stomach Mucosa stomach
10 chr10:22771200-22772800 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
11 chr10:22771400-22771800 Enhancers ES-I3 Cell Line embryonic stem cell
12 chr10:22771400-22771800 Enhancers Psoas Muscle Psoas
13 chr10:22771400-22775600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr10:22771600-22775200 Weak transcription Brain Inferior Temporal Lobe brain
15 chr10:22771600-22779800 Weak transcription Brain Substantia Nigra brain

Quick Search:


  
Input of quick search could be:

what's new

Quick links