Variant report

Variant rs419991
Chromosome Location chr6:145864212-145864213
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:145861400-145869200 Weak transcription Left Ventricle heart
2 chr6:145861600-145864800 Weak transcription NHEK skin
3 chr6:145861600-145865000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr6:145861800-145864800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr6:145861800-145864800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr6:145861800-145865000 Weak transcription Fetal Adrenal Gland Adrenal Gland
7 chr6:145862200-145864400 Weak transcription HMEC breast
8 chr6:145862400-145864400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr6:145862400-145864800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr6:145864200-145865000 Enhancers Pancreatic Islets Pancreatic Islet

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