Variant report

Variant rs9691575
Chromosome Location chr7:16981849-16981850
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:16973600-16982200 Enhancers Primary hematopoietic stem cells short term culture blood
2 chr7:16974400-16982000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr7:16974800-16982000 Weak transcription Pancreas Pancrea
4 chr7:16975600-16987800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr7:16976400-16982200 Enhancers Primary T cells from cord blood blood
6 chr7:16979000-16982000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr7:16979200-16982600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr7:16980000-16982000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr7:16981000-16982000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr7:16981200-16982400 Enhancers HUVEC blood vessel
11 chr7:16981200-16983600 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr7:16981800-16982000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --

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