Variant report

Variant rs6904477
Chromosome Location chr6:35120994-35120995
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:35116800-35121600 Weak transcription GM12878-XiMat blood
2 chr6:35116800-35129200 Weak transcription Aorta Aorta
3 chr6:35118400-35121200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr6:35118600-35132200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr6:35119200-35123600 Enhancers Osteobl bone
6 chr6:35119200-35123800 Enhancers Muscle Satellite Cultured Cells --
7 chr6:35119400-35121200 Enhancers HMEC breast
8 chr6:35119400-35123800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr6:35119600-35121600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr6:35120000-35121200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr6:35120000-35123000 Enhancers NHDF-Ad bronchial
12 chr6:35120000-35123400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr6:35120400-35121800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr6:35120800-35121000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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