Variant report

Variant rs4873284
Chromosome Location chr8:49552970-49552971
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49534400-49556000 Weak transcription Pancreas Pancrea
2 chr8:49544400-49555400 Weak transcription Osteobl bone
3 chr8:49546600-49554400 Weak transcription Fetal Adrenal Gland Adrenal Gland
4 chr8:49547400-49553400 Weak transcription Fetal Lung lung
5 chr8:49549400-49553400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr8:49550200-49555800 Enhancers Placenta Amnion Placenta Amnion
7 chr8:49550400-49554200 Weak transcription Placenta Placenta
8 chr8:49550400-49556000 Weak transcription NH-A brain
9 chr8:49550800-49553000 Weak transcription NHEK skin
10 chr8:49551200-49560800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr8:49551200-49563400 Enhancers Ovary ovary
12 chr8:49551400-49553000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr8:49551400-49553000 Weak transcription HMEC breast
14 chr8:49552000-49553200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr8:49552000-49556200 Weak transcription Left Ventricle heart
16 chr8:49552200-49555400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
17 chr8:49552800-49553200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
18 chr8:49552800-49553600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links