Variant report

Variant rs56354231
Chromosome Location chr6:44776209-44776210
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:44772600-44776800 Weak transcription Primary T cells from cord blood blood
2 chr6:44775000-44777000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr6:44775800-44776400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr6:44775800-44776400 Enhancers NH-A brain
5 chr6:44776000-44776800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr6:44776000-44777000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr6:44776200-44776400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr6:44776200-44777200 Enhancers HUES6 Cell Line embryonic stem cell
9 chr6:44776200-44777200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr6:44776200-44777200 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr6:44776200-44777200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
12 chr6:44776200-44777800 Enhancers ES-I3 Cell Line embryonic stem cell
13 chr6:44776200-44779000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links