Variant report

Variant rs200462868
Chromosome Location chr17:18283746-18283747
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:18267200-18288200 Weak transcription Right Atrium heart
2 chr17:18280400-18284200 Enhancers Stomach Mucosa stomach
3 chr17:18280600-18283800 Enhancers Placenta Placenta
4 chr17:18281400-18286400 Weak transcription Gastric stomach
5 chr17:18281600-18283800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr17:18282600-18283800 Enhancers Esophagus oesophagus
7 chr17:18283000-18283800 Enhancers Rectal Mucosa Donor 29 rectum
8 chr17:18283000-18283800 Bivalent Enhancer NHEK skin
9 chr17:18283000-18288200 Enhancers Fetal Thymus thymus
10 chr17:18283200-18283800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr17:18283400-18283800 Enhancers HUES6 Cell Line embryonic stem cell
12 chr17:18283400-18287000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr17:18283600-18283800 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
14 chr17:18283600-18284000 Enhancers ES-WA7 Cell Line embryonic stem cell
15 chr17:18283600-18284000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
16 chr17:18283600-18284000 Bivalent Enhancer Primary monocytes fromperipheralblood blood
17 chr17:18283600-18284000 Bivalent Enhancer Monocytes-CD14+_RO01746 blood

Quick Search:


  
Input of quick search could be:

what's new

Quick links