Variant report

Variant rs61211228
Chromosome Location chr6:36553416-36553417
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:36551600-36558000 Weak transcription NHDF-Ad bronchial
2 chr6:36551600-36559600 Weak transcription Primary T helper naive cells fromperipheralblood blood
3 chr6:36551600-36560000 Weak transcription Primary T helper cells fromperipheralblood blood
4 chr6:36551600-36560600 Weak transcription Fetal Intestine Small intestine
5 chr6:36552000-36553800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
6 chr6:36552400-36554600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr6:36552800-36553800 Enhancers Muscle Satellite Cultured Cells --
8 chr6:36553000-36553800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr6:36553000-36553800 Enhancers HSMM muscle
10 chr6:36553000-36553800 Enhancers Osteobl bone
11 chr6:36553400-36557400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr6:36553400-36558000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr6:36553400-36558000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr6:36553400-36558000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr6:36553400-36558000 Weak transcription HSMMtube muscle
16 chr6:36553400-36558000 Weak transcription NH-A brain
17 chr6:36553400-36561000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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