Variant report

Variant rs73027827
Chromosome Location chr2:168042484-168042485
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:168037800-168043800 Weak transcription Gastric stomach
2 chr2:168038600-168042600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr2:168038800-168046200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr2:168039000-168043800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr2:168039000-168048000 Weak transcription NHEK skin
6 chr2:168039000-168053000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:168039200-168046200 Weak transcription HMEC breast
8 chr2:168039200-168048000 Weak transcription NHLF lung
9 chr2:168040400-168043000 Weak transcription Fetal Brain Female brain
10 chr2:168041000-168042800 Weak transcription Cortex derived primary cultured neurospheres brain
11 chr2:168041200-168043000 Weak transcription Left Ventricle heart
12 chr2:168041600-168043000 Weak transcription Fetal Brain Male brain
13 chr2:168042400-168048000 Enhancers Breast Myoepithelial Primary Cells Breast

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