Variant report

Variant rs12218657
Chromosome Location chr10:18507688-18507689
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:18499200-18511000 Weak transcription Aorta Aorta
2 chr10:18502400-18513600 Weak transcription Right Ventricle heart
3 chr10:18504400-18508400 Weak transcription Brain Anterior Caudate brain
4 chr10:18504400-18510400 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr10:18504800-18513400 Weak transcription Rectal Smooth Muscle rectum
6 chr10:18505400-18513400 Weak transcription Colon Smooth Muscle Colon
7 chr10:18505600-18508400 Weak transcription Stomach Smooth Muscle stomach
8 chr10:18506000-18512800 Weak transcription Fetal Lung lung
9 chr10:18506200-18513600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr10:18506800-18513600 Weak transcription Pancreas Pancrea
11 chr10:18507000-18508000 Weak transcription Fetal Adrenal Gland Adrenal Gland
12 chr10:18507000-18508400 Weak transcription Left Ventricle heart
13 chr10:18507000-18513600 Weak transcription Ovary ovary
14 chr10:18507200-18509600 Weak transcription Fetal Heart heart
15 chr10:18507400-18507800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr10:18507400-18508600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr10:18507400-18508600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr10:18507600-18508800 Enhancers NHEK skin

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