Variant report

Variant rs57787171
Chromosome Location chr13:50388639-50388640
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:50383600-50389400 Enhancers Fetal Heart heart
2 chr13:50384200-50390200 Enhancers Fetal Adrenal Gland Adrenal Gland
3 chr13:50384800-50389600 Weak transcription Placenta Placenta
4 chr13:50385000-50389400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr13:50386000-50390400 Enhancers HepG2 liver
6 chr13:50387400-50394600 Weak transcription H9 Cell Line embryonic stem cell
7 chr13:50387400-50394800 Weak transcription Fetal Intestine Large intestine
8 chr13:50387600-50388800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
9 chr13:50388200-50389000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr13:50388200-50389000 Weak transcription Skeletal Muscle Female skeletal muscle
11 chr13:50388200-50390000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
12 chr13:50388400-50388800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
13 chr13:50388400-50388800 Weak transcription Left Ventricle heart

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