Variant report

Variant rs524392
Chromosome Location chr11:121066195-121066196
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:121058800-121069000 Weak transcription HUES6 Cell Line embryonic stem cell
2 chr11:121062600-121070000 Weak transcription Fetal Heart heart
3 chr11:121064600-121069000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr11:121065400-121066400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr11:121065400-121066400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
6 chr11:121065600-121066200 Active TSS Brain Inferior Temporal Lobe brain
7 chr11:121065600-121066200 Enhancers Fetal Kidney kidney
8 chr11:121065800-121066200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr11:121065800-121066200 Bivalent Enhancer Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr11:121065800-121070200 Weak transcription H9 Cell Line embryonic stem cell
11 chr11:121066000-121066200 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr11:121066000-121066200 Enhancers HSMMtube muscle
13 chr11:121066000-121066200 Enhancers HUVEC blood vessel
14 chr11:121066000-121067600 Weak transcription iPS-18 Cell Line embryonic stem cell
15 chr11:121066000-121068800 Weak transcription HUES64 Cell Line embryonic stem cell
16 chr11:121066000-121068800 Weak transcription iPS-15b Cell Line embryonic stem cell
17 chr11:121066000-121068800 Weak transcription iPS-20b Cell Line embryonic stem cell
18 chr11:121066000-121069200 Weak transcription H1 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links