Variant report

Variant rs144627656
Chromosome Location chr6:49306769-49306770
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:49295000-49310200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr6:49295400-49309400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr6:49304800-49306800 Weak transcription Aorta Aorta
4 chr6:49304800-49310400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr6:49305000-49307800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr6:49306200-49307400 ZNF genes & repeats HUES64 Cell Line embryonic stem cell
7 chr6:49306400-49307200 Weak transcription H9 Cell Line embryonic stem cell
8 chr6:49306400-49307400 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
9 chr6:49306600-49307200 Weak transcription iPS-15b Cell Line embryonic stem cell

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