Variant report

Variant rs28377198
Chromosome Location chr17:16722552-16722553
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:16716600-16723200 Weak transcription Right Atrium heart
2 chr17:16719000-16723200 Weak transcription Spleen Spleen
3 chr17:16719000-16724000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr17:16719200-16723600 Weak transcription NHEK skin
5 chr17:16720600-16723000 Strong transcription Placenta Amnion Placenta Amnion
6 chr17:16720600-16723200 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr17:16721400-16724600 Enhancers Adipose Nuclei Adipose
8 chr17:16721600-16723800 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr17:16722000-16722600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr17:16722000-16723200 Enhancers Skeletal Muscle Male skeletal muscle
11 chr17:16722000-16724800 Enhancers Right Ventricle heart
12 chr17:16722200-16723000 Bivalent Enhancer Fetal Muscle Leg muscle
13 chr17:16722200-16724200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr17:16722400-16722600 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
15 chr17:16722400-16722800 Genic enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr17:16722400-16722800 Enhancers Brain Dorsolateral Prefrontal Cortex brain
17 chr17:16722400-16723400 Enhancers Skeletal Muscle Female skeletal muscle

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