Variant report

Variant rs74343779
Chromosome Location chr9:16455017-16455018
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:16421800-16460400 Weak transcription Aorta Aorta
2 chr9:16437400-16459200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr9:16438800-16458800 Weak transcription HSMM muscle
4 chr9:16442800-16455800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr9:16446000-16458800 Weak transcription NHLF lung
6 chr9:16446400-16458800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr9:16447000-16457600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr9:16447000-16458400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:16449200-16459200 Weak transcription iPS-15b Cell Line embryonic stem cell
10 chr9:16451000-16456400 Weak transcription Ovary ovary
11 chr9:16451000-16458000 Weak transcription Stomach Smooth Muscle stomach
12 chr9:16452200-16457800 Weak transcription Colon Smooth Muscle Colon
13 chr9:16452200-16458600 Weak transcription Rectal Smooth Muscle rectum
14 chr9:16453800-16457400 Weak transcription GM12878-XiMat blood
15 chr9:16453800-16458600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
16 chr9:16454000-16455600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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