Variant report

Variant rs60361159
Chromosome Location chr2:168042768-168042769
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:168037800-168043800 Weak transcription Gastric stomach
2 chr2:168038800-168046200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr2:168039000-168043800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr2:168039000-168048000 Weak transcription NHEK skin
5 chr2:168039000-168053000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:168039200-168046200 Weak transcription HMEC breast
7 chr2:168039200-168048000 Weak transcription NHLF lung
8 chr2:168040400-168043000 Weak transcription Fetal Brain Female brain
9 chr2:168041000-168042800 Weak transcription Cortex derived primary cultured neurospheres brain
10 chr2:168041200-168043000 Weak transcription Left Ventricle heart
11 chr2:168041600-168043000 Weak transcription Fetal Brain Male brain
12 chr2:168042400-168048000 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr2:168042600-168043200 Enhancers Skeletal Muscle Male skeletal muscle
14 chr2:168042600-168043400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
15 chr2:168042600-168044000 Enhancers Rectal Smooth Muscle rectum
16 chr2:168042600-168044800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

Quick Search:


  
Input of quick search could be:

what's new

Quick links