Variant report

Variant rs528085293
Chromosome Location chr12:57335177-57335178
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:57325800-57335200 Weak transcription Fetal Intestine Large intestine
2 chr12:57326400-57335200 Weak transcription Placenta Amnion Placenta Amnion
3 chr12:57327000-57335200 Weak transcription Spleen Spleen
4 chr12:57329400-57335200 Weak transcription A549 lung
5 chr12:57330000-57335200 Weak transcription K562 blood
6 chr12:57330200-57335200 Weak transcription Esophagus oesophagus
7 chr12:57334600-57336400 Enhancers HMEC breast
8 chr12:57335000-57335200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr12:57335000-57335200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr12:57335000-57335200 Enhancers Muscle Satellite Cultured Cells --
11 chr12:57335000-57335200 Enhancers HepG2 liver
12 chr12:57335000-57335200 Enhancers NHEK skin
13 chr12:57335000-57335600 Enhancers GM12878-XiMat blood
14 chr12:57335000-57336200 Enhancers Skeletal Muscle Male skeletal muscle
15 chr12:57335000-57336400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr12:57335000-57336400 Enhancers Primary hematopoietic stem cells short term culture blood
17 chr12:57335000-57336400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
18 chr12:57335000-57336400 Enhancers HSMM muscle
19 chr12:57335000-57337200 Enhancers Liver Liver

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