Variant report

Variant rs4711121
Chromosome Location chr6:26756442-26756443
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:26747600-26757400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr6:26755600-26756600 Flanking Active TSS K562 blood
3 chr6:26755600-26756800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr6:26756000-26756600 Bivalent Enhancer hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr6:26756000-26757200 Weak transcription HMEC breast
6 chr6:26756200-26756800 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
7 chr6:26756200-26757200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr6:26756400-26756800 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
9 chr6:26756400-26758800 Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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