Variant report

Variant rs28886569
Chromosome Location chr8:100263812-100263813
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:100207000-100290400 Weak transcription Primary T helper cells fromperipheralblood blood
2 chr8:100214800-100293200 Weak transcription Primary T cells fromperipheralblood blood
3 chr8:100232000-100267400 Weak transcription Left Ventricle heart
4 chr8:100246400-100288200 Weak transcription Primary T cells from cord blood blood
5 chr8:100246600-100267000 Weak transcription Primary B cells from cord blood blood
6 chr8:100246800-100266800 Weak transcription Fetal Intestine Small intestine
7 chr8:100252000-100269200 Weak transcription Ovary ovary
8 chr8:100253400-100292400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr8:100260200-100267800 Weak transcription Psoas Muscle Psoas
10 chr8:100260800-100268000 Weak transcription Stomach Smooth Muscle stomach
11 chr8:100261400-100272800 Weak transcription Sigmoid Colon Sigmoid Colon
12 chr8:100262600-100264200 Enhancers HUES48 Cell Line embryonic stem cell
13 chr8:100263200-100264600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr8:100263400-100264000 Enhancers iPS-18 Cell Line embryonic stem cell
15 chr8:100263600-100287800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr8:100263800-100264800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

Quick Search:


  
Input of quick search could be:

what's new

Quick links