Variant report

Variant rs73399822
Chromosome Location chr18:11767930-11767931
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 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 chr18:11765000-11768200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr18:11765800-11768800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
10 chr18:11766600-11768000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr18:11767200-11768400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
12 chr18:11767200-11769000 Weak transcription iPS-15b Cell Line embryonic stem cell
13 chr18:11767400-11768400 Enhancers A549 lung
14 chr18:11767600-11768000 Enhancers Fetal Adrenal Gland Adrenal Gland
15 chr18:11767600-11785400 Weak transcription Breast Myoepithelial Primary Cells Breast
16 chr18:11767600-11789000 Weak transcription Esophagus oesophagus
17 chr18:11767800-11768400 Bivalent Enhancer Muscle Satellite Cultured Cells --
18 chr18:11767800-11769400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
19 chr18:11767800-11771400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
20 chr18:11767800-11783800 Weak transcription H9 Cell Line embryonic stem cell
21 chr18:11767800-11784000 Weak transcription Aorta Aorta

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