Variant report

Variant rs71570347
Chromosome Location chr7:102382770-102382771
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:102381600-102388800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr7:102382400-102383000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr7:102382400-102383000 Enhancers K562 blood
4 chr7:102382600-102382800 Enhancers Brain Dorsolateral Prefrontal Cortex brain
5 chr7:102382600-102382800 Enhancers Brain Substantia Nigra brain
6 chr7:102382600-102383000 Enhancers Primary monocytes fromperipheralblood blood
7 chr7:102382600-102383000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr7:102382600-102383000 Enhancers Brain Angular Gyrus brain
9 chr7:102382600-102383000 Enhancers Brain Cingulate Gyrus brain
10 chr7:102382600-102383000 Flanking Active TSS GM12878-XiMat blood
11 chr7:102382600-102383200 Enhancers Brain Hippocampus Middle brain

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