Variant report

Variant rs2117466
Chromosome Location chr9:110898052-110898053
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:110868600-110899800 Weak transcription H9 Cell Line embryonic stem cell
2 chr9:110882000-110904800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr9:110896000-110899800 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr9:110896200-110899800 Weak transcription iPS-15b Cell Line embryonic stem cell
5 chr9:110896200-110900200 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr9:110896400-110904400 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr9:110896400-110905000 Weak transcription iPS-20b Cell Line embryonic stem cell
8 chr9:110896600-110904600 Weak transcription HUES64 Cell Line embryonic stem cell
9 chr9:110897000-110904400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr9:110898000-110904200 Weak transcription Stomach Mucosa stomach

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