Variant report

Variant rs72684102
Chromosome Location chr4:121990008-121990009
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:121975200-121990200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr4:121985000-121991200 Weak transcription Fetal Intestine Small intestine
3 chr4:121989000-121991400 Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
4 chr4:121989200-121994400 Active TSS Left Ventricle heart
5 chr4:121989200-121994600 Active TSS Ovary ovary
6 chr4:121989400-121992200 Active TSS Right Atrium heart
7 chr4:121989800-121990400 Active TSS Lung lung
8 chr4:121989800-121990600 Flanking Active TSS Fetal Lung lung
9 chr4:121989800-121991400 Active TSS Fetal Intestine Large intestine
10 chr4:121989800-121991400 Active TSS Skeletal Muscle Male skeletal muscle
11 chr4:121989800-121991600 Flanking Active TSS H9 Derived Neuron Cultured Cells ES cell derived
12 chr4:121989800-121992000 Active TSS Adipose Nuclei Adipose
13 chr4:121989800-121992000 Active TSS Psoas Muscle Psoas
14 chr4:121989800-121994200 Active TSS NHDF-Ad bronchial
15 chr4:121990000-121990200 Bivalent/Poised TSS Fetal Brain Male brain
16 chr4:121990000-121990200 Enhancers NHLF lung
17 chr4:121990000-121992200 Bivalent/Poised TSS Osteobl bone

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