Variant report

Variant rs553368845
Chromosome Location chr1:113313672-113313673
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:113305600-113320000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr1:113305600-113332800 Weak transcription H9 Cell Line embryonic stem cell
3 chr1:113307400-113316000 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr1:113310600-113320800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:113312400-113313800 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr1:113313000-113313800 Enhancers Primary T helper memory cells from peripheral blood 2 blood
7 chr1:113313000-113314400 Enhancers Stomach Mucosa stomach
8 chr1:113313200-113314000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr1:113313400-113313800 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr1:113313400-113314200 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr1:113313400-113314200 Enhancers H1 Cell Line embryonic stem cell
12 chr1:113313600-113313800 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr1:113313600-113314200 Enhancers HUES6 Cell Line embryonic stem cell
14 chr1:113313600-113314200 Bivalent Enhancer Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr1:113313600-113314400 Enhancers iPS-15b Cell Line embryonic stem cell

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