Variant report

Variant rs11165813
Chromosome Location chr1:92392134-92392135
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:92386000-92393200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr1:92389800-92393000 Weak transcription Primary Natural Killer cells fromperipheralblood blood
3 chr1:92390000-92392200 Enhancers Hela-S3 cervix
4 chr1:92390200-92392800 Weak transcription HepG2 liver
5 chr1:92390200-92394800 Weak transcription Osteobl bone
6 chr1:92390600-92393800 Weak transcription NHDF-Ad bronchial
7 chr1:92391400-92392400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
8 chr1:92391800-92392200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr1:92391800-92393200 Weak transcription Fetal Adrenal Gland Adrenal Gland
10 chr1:92391800-92393800 Weak transcription Fetal Heart heart
11 chr1:92391800-92394800 Weak transcription Fetal Muscle Leg muscle
12 chr1:92392000-92393000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr1:92392000-92393000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr1:92392000-92394600 Weak transcription NHLF lung

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