Variant report

Variant rs10082872
Chromosome Location chr12:11788661-11788662
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:11787000-11788800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr12:11787000-11789000 Enhancers NHEK skin
3 chr12:11787000-11789200 Enhancers HMEC breast
4 chr12:11787600-11791000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr12:11787600-11791200 Weak transcription Osteobl bone
6 chr12:11788000-11789000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr12:11788200-11788800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr12:11788200-11789200 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
9 chr12:11788200-11790000 ZNF genes & repeats ES-I3 Cell Line embryonic stem cell
10 chr12:11788200-11790000 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
11 chr12:11788600-11789200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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