Variant report

Variant rs6564706
Chromosome Location chr16:79842886-79842887
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:79839000-79844200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr16:79839800-79844800 Weak transcription K562 blood
3 chr16:79840000-79844200 Weak transcription H1 Cell Line embryonic stem cell
4 chr16:79841600-79843000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr16:79841600-79843200 Enhancers NHEK skin
6 chr16:79841600-79844200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr16:79841800-79844800 Weak transcription Fetal Lung lung
8 chr16:79842000-79843600 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr16:79842400-79843000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr16:79842600-79843000 Enhancers HMEC breast
11 chr16:79842800-79844200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr16:79842800-79844200 Weak transcription Esophagus oesophagus
13 chr16:79842800-79844200 Weak transcription Fetal Thymus thymus

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