Variant report

Variant rs17079347
Chromosome Location chr8:2959956-2959957
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:2950800-2965000 Weak transcription K562 blood
2 chr8:2958400-2961200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
3 chr8:2958400-2970400 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr8:2959200-2960400 Enhancers Fetal Kidney kidney
5 chr8:2959400-2961200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr8:2959600-2961000 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr8:2959800-2960000 Enhancers H1 Cell Line embryonic stem cell
8 chr8:2959800-2960200 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
9 chr8:2959800-2960200 Flanking Active TSS iPS-20b Cell Line embryonic stem cell
10 chr8:2959800-2960200 Enhancers Fetal Lung lung
11 chr8:2959800-2960600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
12 chr8:2959800-2960800 Enhancers HUES48 Cell Line embryonic stem cell
13 chr8:2959800-2960800 Enhancers HUES64 Cell Line embryonic stem cell
14 chr8:2959800-2961000 Enhancers H9 Cell Line embryonic stem cell

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