Variant report

Variant rs12898290
Chromosome Location chr15:31294343-31294344
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:31285000-31294800 Weak transcription H9 Cell Line embryonic stem cell
2 chr15:31291800-31308000 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr15:31292800-31294600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr15:31292800-31296200 Enhancers Primary B cells from peripheral blood blood
5 chr15:31293000-31294400 Enhancers GM12878-XiMat blood
6 chr15:31293000-31294600 Enhancers HMEC breast
7 chr15:31293200-31294600 Enhancers NHEK skin
8 chr15:31293200-31294800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr15:31293600-31294400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr15:31293600-31294400 Enhancers Esophagus oesophagus
11 chr15:31293600-31294600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr15:31293600-31298400 Strong transcription Foreskin Melanocyte Primary Cells skin01 Skin
13 chr15:31294000-31294600 Bivalent Enhancer Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr15:31294200-31294400 Flanking Active TSS H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr15:31294200-31294400 Bivalent Enhancer IMR90 fetal lung fibroblasts Cell Line lung
16 chr15:31294200-31294400 Enhancers Placenta Placenta
17 chr15:31294200-31294600 Bivalent/Poised TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
18 chr15:31294200-31294600 Flanking Bivalent TSS/Enh NHDF-Ad bronchial
19 chr15:31294200-31296600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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