Variant report

Variant rs7741888
Chromosome Location chr6:36552304-36552305
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:36548000-36553000 Weak transcription HSMM muscle
2 chr6:36548000-36553000 Weak transcription HSMMtube muscle
3 chr6:36548000-36553000 Weak transcription NH-A brain
4 chr6:36548200-36553000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
5 chr6:36550200-36552400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr6:36551600-36552400 Weak transcription NHEK skin
7 chr6:36551600-36552800 Weak transcription Muscle Satellite Cultured Cells --
8 chr6:36551600-36553000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr6:36551600-36553000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr6:36551600-36553000 Weak transcription Osteobl bone
11 chr6:36551600-36558000 Weak transcription NHDF-Ad bronchial
12 chr6:36551600-36559600 Weak transcription Primary T helper naive cells fromperipheralblood blood
13 chr6:36551600-36560000 Weak transcription Primary T helper cells fromperipheralblood blood
14 chr6:36551600-36560600 Weak transcription Fetal Intestine Small intestine
15 chr6:36551800-36552800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr6:36551800-36553000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr6:36551800-36553000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
18 chr6:36552000-36553800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin

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