Variant report

Variant rs7017560
Chromosome Location chr8:49582651-49582652
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49570000-49584000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr8:49573400-49586000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr8:49580200-49586600 Enhancers Fetal Lung lung
4 chr8:49581200-49587800 Enhancers Fetal Adrenal Gland Adrenal Gland
5 chr8:49581600-49582800 Weak transcription Ovary ovary
6 chr8:49581600-49584000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr8:49581600-49584200 Weak transcription Monocytes-CD14+_RO01746 blood
8 chr8:49581600-49584400 Weak transcription Primary monocytes fromperipheralblood blood
9 chr8:49581800-49582800 Weak transcription Fetal Stomach stomach
10 chr8:49582000-49584600 Enhancers Fetal Kidney kidney
11 chr8:49582200-49583200 Enhancers Aorta Aorta
12 chr8:49582200-49584400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
13 chr8:49582400-49583600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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