Variant report

Variant rs2156665
Chromosome Location chr11:121625327-121625328
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:121613200-121626000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr11:121620800-121632000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr11:121621000-121625400 Weak transcription Rectal Smooth Muscle rectum
4 chr11:121622000-121626200 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr11:121624400-121626000 Enhancers Colon Smooth Muscle Colon
6 chr11:121624600-121626000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr11:121624600-121626200 Enhancers HSMMtube muscle
8 chr11:121624600-121626800 Enhancers Ovary ovary
9 chr11:121624600-121627000 Enhancers Fetal Muscle Leg muscle
10 chr11:121625000-121626200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr11:121625000-121626400 Enhancers Muscle Satellite Cultured Cells --
12 chr11:121625200-121628400 Enhancers Fetal Stomach stomach

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