Variant report

Variant rs11029477
Chromosome Location chr11:26308458-26308459
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:26306600-26308600 Weak transcription NHLF lung
2 chr11:26306600-26309200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr11:26306600-26309800 Weak transcription Fetal Kidney kidney
4 chr11:26306800-26308800 Enhancers ES-I3 Cell Line embryonic stem cell
5 chr11:26307000-26308600 Enhancers iPS-20b Cell Line embryonic stem cell
6 chr11:26307200-26308800 Enhancers ES-WA7 Cell Line embryonic stem cell
7 chr11:26307200-26308800 Enhancers NHDF-Ad bronchial
8 chr11:26308000-26308600 Enhancers HUES64 Cell Line embryonic stem cell
9 chr11:26308200-26308600 Active TSS NH-A brain
10 chr11:26308200-26308800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr11:26308200-26309200 Enhancers Muscle Satellite Cultured Cells --
12 chr11:26308400-26308600 Enhancers HUES48 Cell Line embryonic stem cell
13 chr11:26308400-26308600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr11:26308400-26308600 Enhancers Rectal Smooth Muscle rectum

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