Variant report

Variant rs55996712
Chromosome Location chr6:37768604-37768605
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:37766400-37768800 Enhancers Fetal Stomach stomach
2 chr6:37766400-37775400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr6:37767400-37768800 Enhancers HepG2 liver
4 chr6:37767400-37775400 Weak transcription Skeletal Muscle Female skeletal muscle
5 chr6:37767400-37777000 Weak transcription Right Atrium heart
6 chr6:37767800-37768800 Weak transcription Liver Liver
7 chr6:37767800-37769600 Weak transcription Aorta Aorta
8 chr6:37768400-37769000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr6:37768600-37769000 Enhancers Cortex derived primary cultured neurospheres brain
10 chr6:37768600-37769000 Enhancers Fetal Muscle Trunk muscle
11 chr6:37768600-37769200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
12 chr6:37768600-37769200 Enhancers Fetal Kidney kidney

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