Variant report

Variant rs149119470
Chromosome Location chr5:60117538-60117539
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:60102200-60137800 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr5:60103000-60125600 Weak transcription Brain Angular Gyrus brain
3 chr5:60103000-60129000 Weak transcription Fetal Intestine Small intestine
4 chr5:60106600-60121600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr5:60107000-60122600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr5:60107400-60125600 Weak transcription NHEK skin
7 chr5:60109200-60121400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
8 chr5:60110600-60129000 Weak transcription Fetal Intestine Large intestine
9 chr5:60112600-60120400 Weak transcription Brain Inferior Temporal Lobe brain
10 chr5:60115600-60117600 Enhancers Primary hematopoietic stem cells short term culture blood
11 chr5:60115800-60118600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr5:60116600-60117600 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr5:60116600-60118200 Enhancers GM12878-XiMat blood
14 chr5:60116800-60117600 Enhancers Primary monocytes fromperipheralblood blood
15 chr5:60116800-60117600 Enhancers Monocytes-CD14+_RO01746 blood
16 chr5:60116800-60118400 Enhancers Primary hematopoietic stem cells blood
17 chr5:60117400-60120800 Enhancers K562 blood

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