Variant report

Variant rs10020568
Chromosome Location chr4:53426734-53426735
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:53417800-53427000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr4:53419400-53426800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr4:53421400-53426800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr4:53421600-53434000 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr4:53421800-53426800 Weak transcription Fetal Heart heart
6 chr4:53422000-53426800 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr4:53422000-53426800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr4:53422000-53427000 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr4:53423400-53429800 Weak transcription Gastric stomach
10 chr4:53426400-53427800 Enhancers HMEC breast
11 chr4:53426600-53427600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr4:53426600-53427800 Enhancers Osteobl bone
13 chr4:53426600-53428000 Enhancers NHEK skin

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