Variant report

Variant rs6991747
Chromosome Location chr8:120138193-120138194
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:120134800-120141600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr8:120134800-120141600 Weak transcription NHEK skin
3 chr8:120134800-120141800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr8:120134800-120147600 Weak transcription HMEC breast
5 chr8:120136400-120139000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr8:120136600-120141600 Weak transcription H9 Cell Line embryonic stem cell
7 chr8:120137200-120139000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr8:120138000-120138200 Enhancers Fetal Brain Male brain
9 chr8:120138000-120139400 Enhancers Breast Myoepithelial Primary Cells Breast

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