Variant report

Variant rs35665092
Chromosome Location chr8:86950559-86950560
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:86946400-86951800 Weak transcription Fetal Intestine Small intestine
2 chr8:86947800-86951400 Weak transcription Brain Hippocampus Middle brain
3 chr8:86948600-86950800 Weak transcription Ovary ovary
4 chr8:86949600-86951000 Enhancers K562 blood
5 chr8:86949600-86951800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
6 chr8:86949600-86952400 Enhancers Fetal Lung lung
7 chr8:86949800-86951000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr8:86949800-86951800 Enhancers Fetal Stomach stomach
9 chr8:86950000-86952400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
10 chr8:86950200-86951000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr8:86950200-86951200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr8:86950200-86952200 Enhancers Skeletal Muscle Female skeletal muscle
13 chr8:86950200-86952800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr8:86950200-86952800 Enhancers Primary monocytes fromperipheralblood blood
15 chr8:86950400-86952200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr8:86950400-86952200 Enhancers Monocytes-CD14+_RO01746 blood

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