Variant report

Variant rs8085783
Chromosome Location chr18:11767323-11767324
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:11752800-11774000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr18:11753000-11768000 Weak transcription HMEC breast
3 chr18:11753000-11774800 Weak transcription Stomach Smooth Muscle stomach
4 chr18:11753000-11775400 Weak transcription Gastric stomach
5 chr18:11756600-11769200 Weak transcription Fetal Brain Female brain
6 chr18:11758400-11785600 Weak transcription Brain Anterior Caudate brain
7 chr18:11763400-11780400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr18:11764800-11767600 Weak transcription Fetal Adrenal Gland Adrenal Gland
9 chr18:11765000-11768200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr18:11765600-11767800 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr18:11765800-11768800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
12 chr18:11766200-11767600 Enhancers H1 Cell Line embryonic stem cell
13 chr18:11766400-11767800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
14 chr18:11766600-11768000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr18:11766800-11767800 Enhancers H9 Cell Line embryonic stem cell
16 chr18:11766800-11767800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
17 chr18:11767000-11767600 Strong transcription Breast Myoepithelial Primary Cells Breast
18 chr18:11767200-11767400 Genic enhancers Esophagus oesophagus
19 chr18:11767200-11767800 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
20 chr18:11767200-11767800 ZNF genes & repeats Aorta Aorta
21 chr18:11767200-11768400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
22 chr18:11767200-11769000 Weak transcription iPS-15b Cell Line embryonic stem cell

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