Variant report

Variant rs34484888
Chromosome Location chr7:98846049-98846050
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:98823800-98849600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr7:98842800-98846200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr7:98842800-98846200 Weak transcription NH-A brain
4 chr7:98843200-98846200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr7:98843200-98849600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr7:98843200-98851800 Weak transcription NHEK skin
7 chr7:98843400-98846200 Weak transcription HMEC breast
8 chr7:98843400-98846200 Weak transcription HSMM muscle
9 chr7:98845000-98846800 Enhancers Primary monocytes fromperipheralblood blood
10 chr7:98845600-98850400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr7:98846000-98846200 Flanking Active TSS Monocytes-CD14+_RO01746 blood
12 chr7:98846000-98846400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr7:98846000-98846600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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