Variant report

Variant rs59844066
Chromosome Location chr1:246578639-246578640
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246554600-246594800 Weak transcription Right Ventricle heart
2 chr1:246557200-246590800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr1:246560200-246580600 Weak transcription Primary T cells from cord blood blood
4 chr1:246560400-246580200 Weak transcription Primary hematopoietic stem cells short term culture blood
5 chr1:246571000-246580400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:246575800-246580200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr1:246576400-246588600 Weak transcription H9 Cell Line embryonic stem cell
8 chr1:246577200-246588600 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr1:246577200-246588600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
10 chr1:246577200-246588600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr1:246578400-246578800 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr1:246578400-246578800 Flanking Active TSS Osteobl bone
13 chr1:246578600-246580200 Enhancers NHDF-Ad bronchial

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