Variant report

Variant rs16897115
Chromosome Location chr8:99888442-99888443
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:99878400-99896000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr8:99887000-99889400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr8:99887400-99888600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr8:99887400-99889000 Enhancers HMEC breast
5 chr8:99887400-99889000 Enhancers NHEK skin
6 chr8:99887600-99889000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr8:99887800-99889000 Enhancers HSMM muscle
8 chr8:99887800-99889600 Enhancers Ovary ovary
9 chr8:99887800-99890000 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr8:99888000-99889400 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr8:99888000-99894800 Weak transcription A549 lung
12 chr8:99888200-99889000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr8:99888200-99889000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr8:99888200-99895000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr8:99888400-99889400 Weak transcription ES-I3 Cell Line embryonic stem cell

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