Variant report

Variant rs10102037
Chromosome Location chr8:130815151-130815152
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:130811600-130815200 Weak transcription Monocytes-CD14+_RO01746 blood
2 chr8:130813400-130816000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr8:130813600-130815200 Weak transcription Esophagus oesophagus
4 chr8:130814200-130815200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr8:130814200-130815200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr8:130814400-130815200 Weak transcription Adipose Nuclei Adipose
7 chr8:130814400-130820800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr8:130814800-130816000 Enhancers Left Ventricle heart
9 chr8:130814800-130816200 Enhancers Right Atrium heart
10 chr8:130815000-130815400 Enhancers NHEK skin

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