Variant report

Variant rs452332
Chromosome Location chr21:47339368-47339369
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47308000-47343000 Weak transcription Right Atrium heart
2 chr21:47330800-47342200 Weak transcription Brain Hippocampus Middle brain
3 chr21:47333600-47351600 Weak transcription Gastric stomach
4 chr21:47334400-47340000 Weak transcription Thymus Thymus
5 chr21:47336400-47341800 Weak transcription Primary T helper naive cells fromperipheralblood blood
6 chr21:47336400-47341800 Weak transcription Primary T helper cells PMA-I stimulated --
7 chr21:47336400-47341800 Weak transcription Primary T helper cells fromperipheralblood blood
8 chr21:47336800-47339600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr21:47336800-47342600 Weak transcription Fetal Thymus thymus
10 chr21:47337400-47340600 Weak transcription Muscle Satellite Cultured Cells --
11 chr21:47337400-47341800 Weak transcription Primary T killer naive cells fromperipheralblood blood
12 chr21:47338800-47340200 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr21:47339000-47339400 Enhancers Placenta Placenta
14 chr21:47339000-47339800 Enhancers Spleen Spleen
15 chr21:47339000-47340800 Enhancers Breast Myoepithelial Primary Cells Breast
16 chr21:47339200-47340800 Enhancers Primary Natural Killer cells fromperipheralblood blood

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