Variant report

Variant rs3859192
Chromosome Location chr17:38128648-38128649
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:38110800-38128800 Weak transcription Gastric stomach
2 chr17:38122200-38130600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr17:38122200-38130600 Enhancers Primary monocytes fromperipheralblood blood
4 chr17:38124000-38129600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr17:38124000-38134600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr17:38127400-38129200 Bivalent Enhancer Primary hematopoietic stem cells short term culture blood
7 chr17:38127800-38129000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr17:38127800-38130200 Weak transcription Placenta Placenta
9 chr17:38128000-38129000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
10 chr17:38128000-38129600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr17:38128000-38131400 Enhancers Primary neutrophils fromperipheralblood blood
12 chr17:38128200-38128800 Weak transcription Brain Hippocampus Middle brain
13 chr17:38128200-38128800 Enhancers HSMM muscle
14 chr17:38128200-38129000 Enhancers Primary B cells from peripheral blood blood
15 chr17:38128200-38129000 Flanking Active TSS K562 blood
16 chr17:38128400-38129000 Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr17:38128400-38129000 Enhancers Primary B cells from cord blood blood
18 chr17:38128400-38130400 Enhancers Osteobl bone
19 chr17:38128600-38128800 Enhancers NH-A brain
20 chr17:38128600-38128800 Bivalent Enhancer NHDF-Ad bronchial
21 chr17:38128600-38129000 Flanking Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
22 chr17:38128600-38129200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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