Variant report

Variant rs73544073
Chromosome Location chr6:132625921-132625922
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:132612600-132626400 Weak transcription Fetal Stomach stomach
2 chr6:132615800-132635400 Weak transcription Fetal Lung lung
3 chr6:132617200-132627600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
4 chr6:132617600-132626200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr6:132618400-132631600 Weak transcription Fetal Kidney kidney
6 chr6:132618600-132626200 Weak transcription Osteobl bone
7 chr6:132618800-132634600 Weak transcription NHDF-Ad bronchial
8 chr6:132624600-132627800 Strong transcription Cortex derived primary cultured neurospheres brain
9 chr6:132625000-132627600 Weak transcription Fetal Brain Female brain
10 chr6:132625200-132626800 Strong transcription Foreskin Fibroblast Primary Cells skin02 Skin
11 chr6:132625200-132627000 Strong transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr6:132625200-132627800 Strong transcription Ganglion Eminence derived primary cultured neurospheres brain
13 chr6:132625800-132626000 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr6:132625800-132626200 Genic enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr6:132625800-132626600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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