Variant report

Variant rs11923602
Chromosome Location chr3:56481177-56481178
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:56469000-56492600 Weak transcription H9 Cell Line embryonic stem cell
2 chr3:56478000-56486800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr3:56480400-56481800 Weak transcription iPS-18 Cell Line embryonic stem cell
4 chr3:56480800-56481200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
5 chr3:56481000-56481200 Enhancers Brain Substantia Nigra brain
6 chr3:56481000-56481400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr3:56481000-56481400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr3:56481000-56481400 Enhancers Pancreas Pancrea
9 chr3:56481000-56481600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr3:56481000-56481600 Active TSS iPS-15b Cell Line embryonic stem cell
11 chr3:56481000-56481600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
12 chr3:56481000-56481600 Enhancers Brain Angular Gyrus brain
13 chr3:56481000-56481600 Enhancers Brain Hippocampus Middle brain
14 chr3:56481000-56481600 Enhancers Brain Inferior Temporal Lobe brain
15 chr3:56481000-56481600 Enhancers Fetal Muscle Leg muscle
16 chr3:56481000-56481600 Bivalent Enhancer Placenta Placenta

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