Variant report

Variant rs4529466
Chromosome Location chr8:8121009-8121010
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:8113800-8121200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr8:8117200-8121200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr8:8117600-8124600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr8:8117600-8131200 Weak transcription Placenta Amnion Placenta Amnion
5 chr8:8120200-8127800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr8:8120200-8128000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr8:8120400-8122600 Weak transcription Fetal Lung lung
8 chr8:8120600-8121600 Enhancers HMEC breast
9 chr8:8120800-8121800 Enhancers HepG2 liver
10 chr8:8120800-8125800 Weak transcription Esophagus oesophagus
11 chr8:8120800-8131400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr8:8121000-8121400 Flanking Active TSS A549 lung
13 chr8:8121000-8121600 Enhancers Hela-S3 cervix
14 chr8:8121000-8121600 Enhancers NHEK skin

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