Variant report

Variant rs56260711
Chromosome Location chr8:6766629-6766630
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:6759200-6767000 Weak transcription A549 lung
2 chr8:6761600-6767800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr8:6762800-6766800 Weak transcription Fetal Kidney kidney
4 chr8:6765600-6773600 Enhancers Placenta Placenta
5 chr8:6765800-6766800 Enhancers Esophagus oesophagus
6 chr8:6766000-6768600 Enhancers Placenta Amnion Placenta Amnion
7 chr8:6766200-6768400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr8:6766200-6768600 Enhancers NHEK skin
9 chr8:6766400-6768000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr8:6766400-6768200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr8:6766400-6768600 Enhancers Breast Myoepithelial Primary Cells Breast
12 chr8:6766400-6768600 Enhancers HMEC breast
13 chr8:6766400-6768800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr8:6766600-6766800 Enhancers HepG2 liver

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