Variant report

Variant rs12388560
Chromosome Location chrX:104890141-104890142
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:104887800-104890800 Weak transcription Psoas Muscle Psoas
2 chrX:104889200-104890200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chrX:104889400-104890400 Enhancers NHEK skin
4 chrX:104889400-104890800 Enhancers HMEC breast
5 chrX:104889400-104891800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chrX:104889600-104890400 Enhancers Muscle Satellite Cultured Cells --
7 chrX:104889600-104890800 Enhancers HSMM muscle
8 chrX:104889600-104891000 Enhancers HSMMtube muscle
9 chrX:104889800-104890200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chrX:104889800-104890200 Flanking Active TSS Skeletal Muscle Female skeletal muscle
11 chrX:104889800-104892600 Weak transcription Fetal Adrenal Gland Adrenal Gland
12 chrX:104890000-104890200 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
13 chrX:104890000-104890400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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