Variant report

Variant rs34043867
Chromosome Location chr9:117284862-117284863
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:117275800-117287600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:117278200-117285400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr9:117281400-117289000 Weak transcription Duodenum Mucosa Duodenum
4 chr9:117284400-117285200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
5 chr9:117284600-117285000 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr9:117284600-117285000 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
7 chr9:117284600-117285000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr9:117284600-117285200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr9:117284600-117285200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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