Variant report

Variant rs12579976
Chromosome Location chr12:46938827-46938828
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:46925200-46940600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr12:46925400-46939000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr12:46925400-46940200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr12:46925600-46940000 Weak transcription NHEK skin
5 chr12:46925800-46940200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr12:46926400-46939000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr12:46928400-46948600 Weak transcription Rectal Smooth Muscle rectum
8 chr12:46930600-46940000 Weak transcription Primary B cells from peripheral blood blood
9 chr12:46930800-46940200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr12:46933200-46940200 Weak transcription GM12878-XiMat blood
11 chr12:46933400-46940400 Weak transcription HepG2 liver
12 chr12:46933800-46939600 Weak transcription Skeletal Muscle Female skeletal muscle
13 chr12:46934000-46939000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr12:46938600-46940000 ZNF genes & repeats Primary hematopoietic stem cells blood
15 chr12:46938600-46941800 Enhancers Primary Natural Killer cells fromperipheralblood blood

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