Variant report

Variant rs4775959
Chromosome Location chr15:51891636-51891637
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:51889400-51909400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr15:51890000-51891800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr15:51890000-51894800 Weak transcription Gastric stomach
4 chr15:51890000-51902000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr15:51891400-51892400 Weak transcription Stomach Mucosa stomach
6 chr15:51891400-51893000 Weak transcription Primary neutrophils fromperipheralblood blood
7 chr15:51891400-51893200 Genic enhancers Primary monocytes fromperipheralblood blood
8 chr15:51891400-51893200 Genic enhancers Monocytes-CD14+_RO01746 blood
9 chr15:51891400-51893600 Enhancers K562 blood
10 chr15:51891400-51895200 Enhancers HMEC breast

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