Variant report

Variant rs9669050
Chromosome Location chr12:46933702-46933703
allele A/C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr12:46929600-46933800 Enhancers Skeletal Muscle Female skeletal muscle
9 chr12:46930000-46933800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr12:46930600-46938600 Weak transcription Primary hematopoietic stem cells blood
11 chr12:46930600-46940000 Weak transcription Primary B cells from peripheral blood blood
12 chr12:46930800-46938600 Weak transcription Primary Natural Killer cells fromperipheralblood blood
13 chr12:46930800-46940200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
14 chr12:46933200-46940200 Weak transcription GM12878-XiMat blood
15 chr12:46933400-46933800 Enhancers iPS-18 Cell Line embryonic stem cell
16 chr12:46933400-46934600 Weak transcription ES-I3 Cell Line embryonic stem cell
17 chr12:46933400-46940400 Weak transcription HepG2 liver

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