Variant report

Variant rs16892234
Chromosome Location chr8:120216957-120216958
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:120212800-120218600 Weak transcription Esophagus oesophagus
2 chr8:120215200-120217200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
3 chr8:120215200-120217600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr8:120215200-120219400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr8:120215200-120220000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr8:120215400-120217000 Enhancers NHEK skin
7 chr8:120215400-120219600 Enhancers HMEC breast
8 chr8:120215400-120219800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr8:120215600-120217600 Enhancers Placenta Amnion Placenta Amnion
10 chr8:120215600-120219400 Enhancers Stomach Mucosa stomach
11 chr8:120215800-120217200 Enhancers Adipose Nuclei Adipose
12 chr8:120216000-120217600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
13 chr8:120216200-120219400 Enhancers Hela-S3 cervix
14 chr8:120216200-120220000 Weak transcription Liver Liver
15 chr8:120216400-120220000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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