Variant report

Variant rs17705666
Chromosome Location chr7:17531024-17531025
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17499400-17544600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr7:17528200-17532800 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr7:17528400-17531200 Enhancers Primary T helper naive cells fromperipheralblood blood
4 chr7:17528400-17533200 Enhancers Primary T cells from cord blood blood
5 chr7:17529200-17535800 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr7:17529600-17531200 Enhancers Primary T helper cells fromperipheralblood blood
7 chr7:17530200-17532000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr7:17530400-17531200 Enhancers Primary T helper cells PMA-I stimulated --
9 chr7:17530400-17531800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr7:17530400-17531800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr7:17530400-17531800 Weak transcription NHEK skin
12 chr7:17530600-17531800 Weak transcription HMEC breast
13 chr7:17531000-17531200 Enhancers Primary T killer memory cells from peripheral blood blood
14 chr7:17531000-17531200 Enhancers HepG2 liver

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