Variant report

Variant rs16896014
Chromosome Location chr8:122782756-122782757
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:122768400-122788200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr8:122779600-122785400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr8:122779800-122787000 Weak transcription Fetal Lung lung
4 chr8:122780600-122783400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr8:122780800-122783000 Enhancers Liver Liver
6 chr8:122781400-122783600 Weak transcription HSMM muscle
7 chr8:122781600-122783600 Weak transcription NHLF lung
8 chr8:122781600-122784000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr8:122781600-122784000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr8:122782400-122784000 Enhancers NHDF-Ad bronchial
11 chr8:122782600-122782800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr8:122782600-122782800 Enhancers Fetal Kidney kidney
13 chr8:122782600-122782800 Enhancers Small Intestine intestine
14 chr8:122782600-122782800 Enhancers A549 lung
15 chr8:122782600-122783000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
16 chr8:122782600-122783200 Enhancers HUES48 Cell Line embryonic stem cell
17 chr8:122782600-122784200 Enhancers Adipose Nuclei Adipose

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