Variant report

Variant rs4788560
Chromosome Location chr16:71874332-71874333
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:71868600-71876400 Weak transcription Fetal Kidney kidney
2 chr16:71870800-71879000 Weak transcription NHEK skin
3 chr16:71871400-71876200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr16:71871400-71879000 Weak transcription HMEC breast
5 chr16:71871600-71879200 Weak transcription Fetal Adrenal Gland Adrenal Gland
6 chr16:71871800-71876200 Weak transcription K562 blood
7 chr16:71874000-71874400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr16:71874000-71874600 Enhancers Hela-S3 cervix
9 chr16:71874000-71874600 Enhancers HepG2 liver
10 chr16:71874000-71874600 Enhancers NHDF-Ad bronchial
11 chr16:71874000-71874800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr16:71874200-71874600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr16:71874200-71875800 Weak transcription Placenta Placenta

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