Variant report

Variant rs137553
Chromosome Location chr22:33328896-33328897
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:33314000-33380800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr22:33314200-33332200 Weak transcription HepG2 liver
3 chr22:33319200-33333000 Weak transcription Fetal Brain Male brain
4 chr22:33325400-33329200 Strong transcription HUES48 Cell Line embryonic stem cell
5 chr22:33325400-33329400 Strong transcription H1 Cell Line embryonic stem cell
6 chr22:33326600-33332200 Weak transcription HUES6 Cell Line embryonic stem cell
7 chr22:33326800-33329000 Strong transcription HUES64 Cell Line embryonic stem cell
8 chr22:33327600-33330600 Weak transcription iPS-18 Cell Line embryonic stem cell
9 chr22:33327600-33332600 Weak transcription iPS-20b Cell Line embryonic stem cell
10 chr22:33328400-33329000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr22:33328400-33330800 Enhancers Placenta Amnion Placenta Amnion
12 chr22:33328600-33335400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr22:33328800-33330000 Weak transcription HMEC breast
14 chr22:33328800-33334600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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