Variant report

Variant rs12946603
Chromosome Location chr17:38864580-38864581
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:38854000-38875800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr17:38860000-38864600 Weak transcription Placenta Placenta
3 chr17:38860000-38890200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr17:38861800-38864600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr17:38863600-38864600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr17:38863600-38865000 Enhancers HUVEC blood vessel
7 chr17:38863800-38864600 Bivalent Enhancer HepG2 liver
8 chr17:38864000-38864600 Enhancers Primary monocytes fromperipheralblood blood
9 chr17:38864000-38864600 Enhancers A549 lung
10 chr17:38864000-38864600 Enhancers NHEK skin
11 chr17:38864000-38864800 Enhancers Placenta Amnion Placenta Amnion
12 chr17:38864000-38864800 Enhancers Right Atrium heart
13 chr17:38864000-38865000 Enhancers Monocytes-CD14+_RO01746 blood
14 chr17:38864000-38865200 Enhancers Adipose Nuclei Adipose
15 chr17:38864200-38864800 Flanking Active TSS Hela-S3 cervix
16 chr17:38864200-38864800 Enhancers HMEC breast
17 chr17:38864200-38865000 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
18 chr17:38864200-38865000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
19 chr17:38864200-38865000 Enhancers Esophagus oesophagus
20 chr17:38864400-38865000 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
21 chr17:38864400-38865000 Enhancers Lung lung

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