Variant report

Variant rs577908047
Chromosome Location chr7:17039496-17039497
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17031200-17047400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr7:17033400-17052600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr7:17033600-17043400 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr7:17033800-17045200 Weak transcription Placenta Placenta
5 chr7:17038400-17039800 Enhancers Primary monocytes fromperipheralblood blood
6 chr7:17038400-17040200 Enhancers Dnd41 blood
7 chr7:17038600-17040200 Weak transcription Esophagus oesophagus
8 chr7:17039000-17039800 Enhancers Primary T helper 17 cells PMA-I stimulated --
9 chr7:17039200-17040000 Enhancers Primary T helper memory cells from peripheral blood 2 blood
10 chr7:17039400-17039800 Flanking Active TSS Primary neutrophils fromperipheralblood blood
11 chr7:17039400-17039800 ZNF genes & repeats Primary B cells from cord blood blood
12 chr7:17039400-17039800 Enhancers Primary T helper cells PMA-I stimulated --
13 chr7:17039400-17039800 Enhancers Primary T helper cells fromperipheralblood blood
14 chr7:17039400-17039800 Enhancers Sigmoid Colon Sigmoid Colon
15 chr7:17039400-17039800 Flanking Active TSS Monocytes-CD14+_RO01746 blood

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