Variant report

Variant rs6938195
Chromosome Location chr6:132649311-132649312
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:132626600-132651400 Weak transcription Fetal Stomach stomach
2 chr6:132635600-132655000 Weak transcription NH-A brain
3 chr6:132637000-132652800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr6:132638800-132654800 Weak transcription Fetal Kidney kidney
5 chr6:132639000-132651200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr6:132640400-132662200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr6:132644000-132657400 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr6:132644400-132675400 Weak transcription Fetal Lung lung
9 chr6:132645000-132655000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr6:132646400-132651600 Strong transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr6:132648000-132649800 Strong transcription NHDF-Ad bronchial
12 chr6:132648200-132654800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
13 chr6:132648800-132651600 Strong transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr6:132649200-132652000 Strong transcription Cortex derived primary cultured neurospheres brain

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