Variant report

Variant rs5998963
Chromosome Location chr22:33880193-33880194
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:33862200-33883000 Weak transcription Brain Inferior Temporal Lobe brain
2 chr22:33864000-33888200 Weak transcription Fetal Stomach stomach
3 chr22:33864000-33888200 Weak transcription Ovary ovary
4 chr22:33873000-33883400 Weak transcription Gastric stomach
5 chr22:33873000-33888000 Weak transcription Pancreas Pancrea
6 chr22:33873000-33888200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr22:33873000-33888200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr22:33874000-33882200 Weak transcription Brain Hippocampus Middle brain
9 chr22:33874000-33882400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr22:33874000-33883200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
11 chr22:33874200-33888200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr22:33874400-33888200 Weak transcription Skeletal Muscle Male skeletal muscle
13 chr22:33875000-33883000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
14 chr22:33875200-33888200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
15 chr22:33878400-33884400 Weak transcription Fetal Brain Female brain
16 chr22:33879400-33880200 Enhancers Fetal Heart heart
17 chr22:33879400-33885000 Weak transcription Aorta Aorta
18 chr22:33879600-33883400 Weak transcription Right Atrium heart
19 chr22:33880000-33880600 Weak transcription Left Ventricle heart
20 chr22:33880000-33883400 Weak transcription Right Ventricle heart

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