Variant report

Variant rs138882491
Chromosome Location chr6:31880053-31880054
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr6:31876200-31880200 Enhancers Fetal Adrenal Gland Adrenal Gland
5 chr6:31876400-31880400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr6:31877400-31884800 Weak transcription Brain Anterior Caudate brain
7 chr6:31877600-31883400 Weak transcription HepG2 liver
8 chr6:31878000-31880200 Enhancers NHDF-Ad bronchial
9 chr6:31878000-31880400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr6:31879000-31880800 Enhancers K562 blood
11 chr6:31879400-31881400 Weak transcription NHEK skin
12 chr6:31879800-31880200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr6:31879800-31880200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
14 chr6:31880000-31881000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr6:31880000-31881800 Weak transcription GM12878-XiMat blood
16 chr6:31880000-31882800 Weak transcription Placenta Placenta
17 chr6:31880000-31884800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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