Variant report

Variant rs7985229
Chromosome Location chr13:111260229-111260230
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:111249800-111262400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr13:111254000-111260400 Weak transcription HepG2 liver
3 chr13:111254000-111262600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr13:111255800-111262600 Weak transcription Placenta Amnion Placenta Amnion
5 chr13:111259600-111262600 Weak transcription H1 Cell Line embryonic stem cell
6 chr13:111259800-111261000 Enhancers Fetal Adrenal Gland Adrenal Gland
7 chr13:111260000-111262600 Weak transcription Placenta Placenta
8 chr13:111260200-111260600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr13:111260200-111260600 Weak transcription Ovary ovary
10 chr13:111260200-111260600 Enhancers GM12878-XiMat blood
11 chr13:111260200-111260800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

Quick Search:


  
Input of quick search could be:

what's new

Quick links