Variant report

Variant rs72636668
Chromosome Location chr8:50709306-50709307
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:50693200-50719600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr8:50706800-50724000 Weak transcription H1 Cell Line embryonic stem cell
3 chr8:50707400-50709600 Enhancers Hela-S3 cervix
4 chr8:50707400-50711000 Enhancers HMEC breast
5 chr8:50707800-50712800 Enhancers HUES64 Cell Line embryonic stem cell
6 chr8:50708000-50711000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr8:50708200-50710400 Enhancers Placenta Amnion Placenta Amnion
8 chr8:50708200-50710800 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr8:50708600-50709400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr8:50708600-50717000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr8:50708800-50710000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr8:50708800-50710800 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr8:50709000-50710000 Weak transcription iPS-15b Cell Line embryonic stem cell
14 chr8:50709000-50712800 Enhancers Cortex derived primary cultured neurospheres brain
15 chr8:50709200-50710200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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