Variant report

Variant rs552979017
Chromosome Location chr12:123182522-123182523
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:123166600-123187800 Weak transcription A549 lung
2 chr12:123174000-123199800 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr12:123181200-123183000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr12:123181200-123183000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr12:123181600-123182600 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr12:123181600-123182600 Enhancers HMEC breast
7 chr12:123181600-123182600 Enhancers NHEK skin
8 chr12:123181800-123185400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr12:123182000-123182600 Enhancers Adipose Nuclei Adipose
10 chr12:123182200-123184200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr12:123182400-123182600 Enhancers Monocytes-CD14+_RO01746 blood
12 chr12:123182400-123182800 Enhancers Primary neutrophils fromperipheralblood blood
13 chr12:123182400-123182800 Weak transcription Placenta Placenta
14 chr12:123182400-123183000 Enhancers Primary T cells from cord blood blood

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