Variant report

Variant rs10975679
Chromosome Location chr9:669386-669387
allele C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:650800-670400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr9:653400-698000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr9:656400-673800 Weak transcription Stomach Smooth Muscle stomach
4 chr9:656600-670400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr9:656600-670400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr9:656800-673800 Weak transcription Psoas Muscle Psoas
7 chr9:657800-672000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr9:657800-673200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr9:658400-672000 Weak transcription Colon Smooth Muscle Colon
10 chr9:664000-670400 Weak transcription Esophagus oesophagus
11 chr9:664000-670400 Weak transcription Left Ventricle heart
12 chr9:664000-673600 Weak transcription A549 lung
13 chr9:664200-673800 Weak transcription Fetal Heart heart
14 chr9:668800-670000 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr9:669200-670400 Weak transcription Fetal Intestine Small intestine

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