Variant report

Variant rs531360145
Chromosome Location chr6:31880356-31880357
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:31874600-31883600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:31874800-31880400 Enhancers Hela-S3 cervix
3 chr6:31875600-31882600 Weak transcription Primary hematopoietic stem cells short term culture blood
4 chr6:31876400-31880400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr6:31877400-31884800 Weak transcription Brain Anterior Caudate brain
6 chr6:31877600-31883400 Weak transcription HepG2 liver
7 chr6:31878000-31880400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr6:31879000-31880800 Enhancers K562 blood
9 chr6:31879400-31881400 Weak transcription NHEK skin
10 chr6:31880000-31881000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr6:31880000-31881800 Weak transcription GM12878-XiMat blood
12 chr6:31880000-31882800 Weak transcription Placenta Placenta
13 chr6:31880000-31884800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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