Variant report

Variant rs35092969
Chromosome Location chr5:44000448-44000449
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:43998000-44002000 Weak transcription Pancreas Pancrea
2 chr5:43998000-44002000 Weak transcription NHLF lung
3 chr5:43998200-44002000 Weak transcription NHDF-Ad bronchial
4 chr5:43998400-44001200 Weak transcription Stomach Mucosa stomach
5 chr5:43998400-44001800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr5:43998400-44002000 Weak transcription Gastric stomach
7 chr5:43998400-44003000 Enhancers Fetal Lung lung
8 chr5:43998400-44005000 Enhancers HepG2 liver
9 chr5:43998600-44002000 Weak transcription Hela-S3 cervix
10 chr5:43998800-44001200 Weak transcription Adipose Nuclei Adipose
11 chr5:43998800-44002000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr5:43998800-44002000 Weak transcription Fetal Adrenal Gland Adrenal Gland
13 chr5:43999000-44001000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr5:44000000-44001200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr5:44000200-44004200 Enhancers Liver Liver

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