Variant report

Variant rs1398354
Chromosome Location chr3:110250796-110250797
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:110246800-110251000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr3:110246800-110251800 Weak transcription Fetal Intestine Small intestine
3 chr3:110247000-110251400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr3:110247400-110251200 Weak transcription Fetal Intestine Large intestine
5 chr3:110247600-110251200 Weak transcription NHDF-Ad bronchial
6 chr3:110247600-110251400 Weak transcription NHLF lung
7 chr3:110247600-110252000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr3:110249000-110250800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr3:110250200-110250800 Enhancers H1 Cell Line embryonic stem cell
10 chr3:110250600-110250800 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr3:110250600-110250800 Enhancers H9 Cell Line embryonic stem cell
12 chr3:110250600-110251000 Enhancers HUES48 Cell Line embryonic stem cell
13 chr3:110250600-110251000 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr3:110250600-110251200 Enhancers iPS-15b Cell Line embryonic stem cell
15 chr3:110250600-110251200 Strong transcription K562 blood

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