Variant report

Variant rs2981892
Chromosome Location chr1:174839048-174839049
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174819200-174843600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr1:174832000-174843000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr1:174833000-174841400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:174836800-174843600 Weak transcription Left Ventricle heart
5 chr1:174837400-174839400 Weak transcription iPS-20b Cell Line embryonic stem cell
6 chr1:174837600-174840400 Weak transcription H9 Cell Line embryonic stem cell
7 chr1:174838600-174840400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr1:174838600-174843400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr1:174838600-174847400 Weak transcription Esophagus oesophagus
10 chr1:174838800-174839600 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr1:174839000-174840800 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr1:174839000-174841000 Weak transcription Primary B cells from cord blood blood
13 chr1:174839000-174841000 Enhancers GM12878-XiMat blood

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