Variant report

Variant rs56150806
Chromosome Location chr17:43919301-43919302
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:43915400-43919800 Enhancers Fetal Brain Male brain
2 chr17:43916200-43920000 Enhancers Fetal Brain Female brain
3 chr17:43917600-43926400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr17:43917800-43920000 Enhancers Brain Germinal Matrix brain
5 chr17:43918800-43919400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr17:43919200-43919400 Enhancers Primary hematopoietic stem cells blood
7 chr17:43919200-43919400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
8 chr17:43919200-43919600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr17:43919200-43919600 Enhancers Brain Hippocampus Middle brain
10 chr17:43919200-43919600 Bivalent Enhancer Fetal Muscle Trunk muscle

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