Variant report

Variant rs10817634
Chromosome Location chr9:117286403-117286404
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:117275800-117287600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:117281400-117289000 Weak transcription Duodenum Mucosa Duodenum
3 chr9:117285000-117287800 Weak transcription A549 lung
4 chr9:117285400-117287400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr9:117285600-117287800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
6 chr9:117286000-117288800 Weak transcription Fetal Intestine Small intestine
7 chr9:117286200-117286800 Flanking Active TSS Stomach Smooth Muscle stomach
8 chr9:117286200-117287400 Enhancers Fetal Muscle Leg muscle
9 chr9:117286200-117288000 Enhancers HSMMtube muscle
10 chr9:117286200-117288200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr9:117286400-117286600 Flanking Active TSS Colon Smooth Muscle Colon
12 chr9:117286400-117286600 Bivalent Enhancer NHLF lung
13 chr9:117286400-117286800 Flanking Active TSS Rectal Smooth Muscle rectum

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