Variant report

Variant rs11941436
Chromosome Location chr4:148017665-148017666
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:148010000-148022800 Weak transcription NHLF lung
2 chr4:148010200-148017800 Weak transcription Osteobl bone
3 chr4:148010400-148021200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr4:148010800-148018000 Weak transcription HUES48 Cell Line embryonic stem cell
5 chr4:148016800-148017800 Enhancers Fetal Heart heart
6 chr4:148017000-148018800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr4:148017200-148018400 Enhancers Hela-S3 cervix
8 chr4:148017400-148018000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr4:148017400-148018000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr4:148017400-148018000 Enhancers Adipose Nuclei Adipose
11 chr4:148017600-148018600 Enhancers Muscle Satellite Cultured Cells --
12 chr4:148017600-148019000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr4:148017600-148022600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr4:148017600-148023000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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