Variant report

Variant rs16937632
Chromosome Location chr8:49445074-49445075
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49428000-49448600 Weak transcription Right Atrium heart
2 chr8:49437200-49445400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr8:49438600-49447600 Weak transcription NHLF lung
4 chr8:49438600-49457400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr8:49439800-49447600 Weak transcription Fetal Lung lung
6 chr8:49440000-49447400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr8:49442800-49448000 Weak transcription Placenta Amnion Placenta Amnion
8 chr8:49443000-49448400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr8:49443000-49455200 Weak transcription ES-WA7 Cell Line embryonic stem cell
10 chr8:49443600-49454600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr8:49443800-49448200 Weak transcription iPS-15b Cell Line embryonic stem cell
12 chr8:49443800-49448200 Weak transcription iPS-18 Cell Line embryonic stem cell
13 chr8:49444000-49447800 Weak transcription HUES64 Cell Line embryonic stem cell
14 chr8:49444000-49448200 Weak transcription HUES48 Cell Line embryonic stem cell
15 chr8:49444000-49448200 Weak transcription iPS-20b Cell Line embryonic stem cell
16 chr8:49444600-49445200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
17 chr8:49444600-49445200 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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