Variant report

Variant rs7999146
Chromosome Location chr13:110491261-110491262
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:110488400-110496200 Weak transcription Aorta Aorta
2 chr13:110489600-110492600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr13:110489600-110497200 Weak transcription Stomach Mucosa stomach
4 chr13:110489800-110491600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr13:110489800-110492000 Weak transcription Dnd41 blood
6 chr13:110489800-110492600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr13:110489800-110492600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr13:110489800-110492600 Weak transcription Pancreas Pancrea
9 chr13:110489800-110492800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
10 chr13:110490000-110491600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr13:110490800-110492400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr13:110491000-110492600 Enhancers Muscle Satellite Cultured Cells --
13 chr13:110491000-110494800 Enhancers HSMM muscle

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