Variant report

Variant rs2141552
Chromosome Location chr4:69279511-69279512
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:69273200-69279600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr4:69276400-69283600 Weak transcription iPS-20b Cell Line embryonic stem cell
3 chr4:69276800-69279600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr4:69276800-69279600 Weak transcription iPS-15b Cell Line embryonic stem cell
5 chr4:69276800-69282200 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr4:69276800-69283400 Weak transcription H1 Cell Line embryonic stem cell
7 chr4:69276800-69284600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr4:69278400-69282200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr4:69278400-69282200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr4:69278600-69280000 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr4:69278600-69282200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr4:69278800-69281600 Weak transcription HMEC breast
13 chr4:69278800-69283400 Weak transcription H9 Cell Line embryonic stem cell
14 chr4:69279200-69280000 Enhancers Placenta Placenta
15 chr4:69279400-69280000 Enhancers HUES48 Cell Line embryonic stem cell
16 chr4:69279400-69280200 Enhancers HUES64 Cell Line embryonic stem cell

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