Variant report

Variant rs373483186
Chromosome Location chr20:22773511-22773512
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:22770400-22775400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr20:22770600-22775800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr20:22771000-22774200 Weak transcription Aorta Aorta
4 chr20:22771000-22774200 Weak transcription Fetal Muscle Leg muscle
5 chr20:22771000-22775400 Weak transcription Fetal Muscle Trunk muscle
6 chr20:22771000-22776000 Weak transcription Ovary ovary
7 chr20:22772000-22778600 Enhancers HMEC breast
8 chr20:22772200-22777400 Enhancers Placenta Placenta
9 chr20:22772800-22775400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr20:22773000-22774000 Weak transcription Placenta Amnion Placenta Amnion
11 chr20:22773000-22774800 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr20:22773000-22774800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr20:22773000-22775000 Weak transcription Primary hematopoietic stem cells short term culture blood
14 chr20:22773200-22773600 Weak transcription Right Atrium heart
15 chr20:22773200-22774200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr20:22773200-22774200 Weak transcription A549 lung
17 chr20:22773200-22774800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr20:22773200-22774800 Weak transcription NHEK skin

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