Variant report

Variant rs4509954
Chromosome Location chr14:104661941-104661942
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104643800-104662200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr14:104656200-104662200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr14:104656200-104669200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr14:104657200-104665400 Weak transcription Fetal Brain Female brain
5 chr14:104661000-104663000 Weak transcription Spleen Spleen
6 chr14:104661200-104663400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr14:104661400-104663600 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr14:104661600-104662000 Weak transcription Fetal Brain Male brain
9 chr14:104661800-104663200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr14:104661800-104663400 Flanking Active TSS Brain Germinal Matrix brain

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