Variant report

Variant rs1356761
Chromosome Location chr8:129805974-129805975
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:129784000-129809800 Weak transcription Dnd41 blood
2 chr8:129801000-129806000 Weak transcription HSMM muscle
3 chr8:129801000-129806600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
4 chr8:129801200-129806000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr8:129801200-129806600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr8:129801400-129806200 Weak transcription NHDF-Ad bronchial
7 chr8:129801400-129806600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr8:129805200-129807600 Enhancers HUVEC blood vessel
9 chr8:129805400-129808200 Enhancers Cortex derived primary cultured neurospheres brain
10 chr8:129805600-129807600 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr8:129805600-129807800 Enhancers Brain Germinal Matrix brain
12 chr8:129805800-129806000 Enhancers Pancreatic Islets Pancreatic Islet
13 chr8:129805800-129807600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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