Variant report

Variant rs9297289
Chromosome Location chr8:100256910-100256911
allele C/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 chr8:100230400-100257800 Weak transcription Aorta Aorta
4 chr8:100232000-100267400 Weak transcription Left Ventricle heart
5 chr8:100246400-100288200 Weak transcription Primary T cells from cord blood blood
6 chr8:100246600-100261000 Weak transcription Primary monocytes fromperipheralblood blood
7 chr8:100246600-100267000 Weak transcription Primary B cells from cord blood blood
8 chr8:100246800-100261000 Weak transcription Monocytes-CD14+_RO01746 blood
9 chr8:100246800-100262000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr8:100246800-100266800 Weak transcription Fetal Intestine Small intestine
11 chr8:100251600-100260000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr8:100252000-100269200 Weak transcription Ovary ovary
13 chr8:100253000-100257000 Weak transcription HUVEC blood vessel
14 chr8:100253200-100263200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr8:100253400-100292400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr8:100254200-100263800 Weak transcription Fetal Lung lung

Quick Search:


  
Input of quick search could be:

what's new

Quick links