Variant report

Variant rs556047912
Chromosome Location chr4:69282265-69282266
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:69276400-69283600 Weak transcription iPS-20b Cell Line embryonic stem cell
2 chr4:69276800-69283400 Weak transcription H1 Cell Line embryonic stem cell
3 chr4:69276800-69284600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr4:69278800-69283400 Weak transcription H9 Cell Line embryonic stem cell
5 chr4:69280000-69286000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr4:69280800-69282600 Weak transcription HUES64 Cell Line embryonic stem cell
7 chr4:69280800-69289600 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr4:69282200-69282400 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr4:69282200-69282600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr4:69282200-69282800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr4:69282200-69282800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr4:69282200-69282800 Enhancers HMEC breast

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