Variant report

Variant rs16937638
Chromosome Location chr8:49445480-49445481
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49428000-49448600 Weak transcription Right Atrium heart
2 chr8:49438600-49447600 Weak transcription NHLF lung
3 chr8:49438600-49457400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr8:49439800-49447600 Weak transcription Fetal Lung lung
5 chr8:49440000-49447400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr8:49442800-49448000 Weak transcription Placenta Amnion Placenta Amnion
7 chr8:49443000-49448400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr8:49443000-49455200 Weak transcription ES-WA7 Cell Line embryonic stem cell
9 chr8:49443600-49454600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr8:49443800-49448200 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chr8:49443800-49448200 Weak transcription iPS-18 Cell Line embryonic stem cell
12 chr8:49444000-49447800 Weak transcription HUES64 Cell Line embryonic stem cell
13 chr8:49444000-49448200 Weak transcription HUES48 Cell Line embryonic stem cell
14 chr8:49444000-49448200 Weak transcription iPS-20b Cell Line embryonic stem cell
15 chr8:49445200-49447000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr8:49445400-49445600 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr8:49445400-49445600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
18 chr8:49445400-49445600 Enhancers Fetal Muscle Trunk muscle
19 chr8:49445400-49445800 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin02 Skin

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