Variant report

Variant rs4742208
Chromosome Location chr9:668240-668241
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr9:661400-668800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr9:664000-670400 Weak transcription Esophagus oesophagus
12 chr9:664000-670400 Weak transcription Left Ventricle heart
13 chr9:664000-673600 Weak transcription A549 lung
14 chr9:664200-673800 Weak transcription Fetal Heart heart
15 chr9:668000-669200 ZNF genes & repeats Fetal Intestine Small intestine
16 chr9:668200-668600 Enhancers Brain Substantia Nigra brain

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