Variant report

Variant rs4392878
Chromosome Location chr8:125054726-125054727
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:125050600-125054800 Enhancers Fetal Intestine Small intestine
2 chr8:125051200-125054800 Enhancers Fetal Intestine Large intestine
3 chr8:125052600-125083600 Weak transcription Gastric stomach
4 chr8:125053000-125060400 Weak transcription Left Ventricle heart
5 chr8:125053600-125058600 Enhancers Fetal Heart heart
6 chr8:125053800-125056200 Weak transcription Duodenum Mucosa Duodenum
7 chr8:125053800-125059800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr8:125053800-125062400 Weak transcription Stomach Mucosa stomach
9 chr8:125054000-125055400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr8:125054200-125056400 Weak transcription Cortex derived primary cultured neurospheres brain
11 chr8:125054200-125056400 Weak transcription A549 lung
12 chr8:125054200-125061000 Weak transcription Fetal Stomach stomach
13 chr8:125054400-125056600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr8:125054400-125056800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
15 chr8:125054600-125066800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --

Quick Search:


  
Input of quick search could be:

what's new

Quick links