Variant report

Variant rs10788715
Chromosome Location chr17:20976220-20976221
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:20970200-20978600 Weak transcription HSMMtube muscle
2 chr17:20973600-20977600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr17:20974200-20978400 Weak transcription HSMM muscle
4 chr17:20975000-20983400 Enhancers Fetal Brain Male brain
5 chr17:20975400-20979000 Enhancers Fetal Muscle Trunk muscle
6 chr17:20975800-20976800 Enhancers Fetal Stomach stomach
7 chr17:20975800-20977000 Enhancers Fetal Muscle Leg muscle
8 chr17:20976000-20976400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr17:20976000-20976600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr17:20976000-20976600 Enhancers Cortex derived primary cultured neurospheres brain
11 chr17:20976200-20976600 Active TSS Brain Germinal Matrix brain
12 chr17:20976200-20976600 Enhancers Brain Hippocampus Middle brain
13 chr17:20976200-20979000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr17:20976200-20989000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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