Variant report

Variant rs9366714
Chromosome Location chr6:28062866-28062867
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:28049600-28063000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
2 chr6:28053400-28064600 Strong transcription Placenta Placenta
3 chr6:28057800-28065800 Weak transcription HUES6 Cell Line embryonic stem cell
4 chr6:28058000-28064800 Weak transcription H9 Cell Line embryonic stem cell
5 chr6:28058200-28072200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr6:28058800-28072000 Weak transcription HMEC breast
7 chr6:28059200-28063000 Weak transcription Placenta Amnion Placenta Amnion
8 chr6:28059200-28063200 Weak transcription Pancreas Pancrea
9 chr6:28059200-28063400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr6:28059200-28066800 Weak transcription Esophagus oesophagus
11 chr6:28059400-28072000 Weak transcription Brain Substantia Nigra brain
12 chr6:28059800-28063600 Weak transcription Fetal Heart heart
13 chr6:28061000-28063800 Weak transcription NHEK skin
14 chr6:28061200-28063600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr6:28061200-28064600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
16 chr6:28061400-28072000 Weak transcription Breast Myoepithelial Primary Cells Breast
17 chr6:28062000-28064600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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