Variant report

Variant rs57773346
Chromosome Location chr8:6779850-6779851
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:6776200-6782400 Enhancers Primary B cells from cord blood blood
2 chr8:6776400-6782800 Enhancers Primary B cells from peripheral blood blood
3 chr8:6778000-6780000 Enhancers Lung lung
4 chr8:6778400-6783400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr8:6779200-6785600 Enhancers Dnd41 blood
6 chr8:6779400-6780000 Bivalent Enhancer Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr8:6779400-6780000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr8:6779400-6780000 Enhancers Rectal Mucosa Donor 31 rectum
9 chr8:6779400-6780000 Enhancers GM12878-XiMat blood
10 chr8:6779400-6780200 Enhancers Fetal Kidney kidney
11 chr8:6779400-6780400 Bivalent Enhancer Rectal Mucosa Donor 29 rectum
12 chr8:6779400-6780600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr8:6779600-6780600 Enhancers Primary Natural Killer cells fromperipheralblood blood
14 chr8:6779800-6781200 Weak transcription HUES6 Cell Line embryonic stem cell
15 chr8:6779800-6786000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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