Variant report

Variant rs143838984
Chromosome Location chr11:75892751-75892752
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:75883600-75897000 Weak transcription Fetal Intestine Small intestine
2 chr11:75887800-75896400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr11:75888200-75895200 Weak transcription HUES6 Cell Line embryonic stem cell
4 chr11:75888800-75894800 Weak transcription Fetal Lung lung
5 chr11:75890600-75897000 Weak transcription Gastric stomach
6 chr11:75890800-75895200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr11:75891000-75896000 Weak transcription Placenta Amnion Placenta Amnion
8 chr11:75891800-75893400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr11:75891800-75893600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr11:75892000-75892800 Strong transcription Fetal Adrenal Gland Adrenal Gland
11 chr11:75892000-75894600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr11:75892200-75892800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr11:75892200-75895200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr11:75892400-75895400 Weak transcription ES-WA7 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links