Variant report

Variant rs1338938
Chromosome Location chr6:132726450-132726451
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:132723400-132726600 Enhancers NHDF-Ad bronchial
2 chr6:132724200-132727800 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr6:132724600-132727000 Flanking Active TSS GM12878-XiMat blood
4 chr6:132724800-132727600 Enhancers Osteobl bone
5 chr6:132725000-132727200 Enhancers NHLF lung
6 chr6:132725200-132727400 Enhancers NH-A brain
7 chr6:132725200-132734800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr6:132725400-132727600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr6:132725600-132726800 Enhancers Muscle Satellite Cultured Cells --
10 chr6:132725600-132727200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr6:132725800-132727000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr6:132726000-132727400 Enhancers HSMM muscle
13 chr6:132726200-132727200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr6:132726400-132726600 Enhancers Stomach Smooth Muscle stomach
15 chr6:132726400-132727800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr6:132726400-132734200 Weak transcription Fetal Kidney kidney

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