Variant report

Variant rs1027589
Chromosome Location chr12:67787928-67787929
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:67782600-67788400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr12:67783000-67788000 Weak transcription NHEK skin
3 chr12:67783200-67788200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr12:67783400-67788000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr12:67785200-67788200 Weak transcription Adipose Nuclei Adipose
6 chr12:67785600-67788200 Weak transcription HSMMtube muscle
7 chr12:67787200-67789000 Enhancers Fetal Muscle Leg muscle
8 chr12:67787600-67788400 Enhancers Skeletal Muscle Female skeletal muscle
9 chr12:67787600-67789400 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr12:67787800-67788200 Weak transcription Psoas Muscle Psoas
11 chr12:67787800-67788400 Enhancers Skeletal Muscle Male skeletal muscle
12 chr12:67787800-67789200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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