Variant report

Variant rs150946021
Chromosome Location chr5:1932608-1932609
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:1932000-1943200 Weak transcription Esophagus oesophagus
2 chr5:1932000-1950800 Weak transcription Gastric stomach
3 chr5:1932200-1932800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr5:1932200-1933000 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr5:1932200-1933200 Weak transcription NHEK skin
6 chr5:1932200-1933400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr5:1932200-1933800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr5:1932200-1934200 Weak transcription Pancreas Pancrea
9 chr5:1932200-1934400 Weak transcription Brain Anterior Caudate brain
10 chr5:1932200-1934400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
11 chr5:1932200-1934800 Weak transcription Ovary ovary
12 chr5:1932200-1935000 Weak transcription Brain Inferior Temporal Lobe brain
13 chr5:1932200-1935000 Weak transcription Left Ventricle heart
14 chr5:1932200-1937600 Weak transcription H9 Cell Line embryonic stem cell
15 chr5:1932200-1937600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
16 chr5:1932200-1942200 Weak transcription Stomach Smooth Muscle stomach
17 chr5:1932200-1945600 Weak transcription Right Ventricle heart
18 chr5:1932200-1946400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
19 chr5:1932400-1936600 Weak transcription Adipose Nuclei Adipose
20 chr5:1932600-1933000 Weak transcription HMEC breast

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