Variant report

Variant rs16938608
Chromosome Location chr8:49621293-49621294
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49605600-49621800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr8:49612800-49626400 Weak transcription Placenta Amnion Placenta Amnion
3 chr8:49616200-49622400 Enhancers Esophagus oesophagus
4 chr8:49617200-49622400 Enhancers Fetal Heart heart
5 chr8:49617600-49621800 Enhancers Right Ventricle heart
6 chr8:49617800-49621600 Enhancers Left Ventricle heart
7 chr8:49618000-49626000 Weak transcription Fetal Kidney kidney
8 chr8:49618200-49621800 Enhancers Right Atrium heart
9 chr8:49618200-49628000 Weak transcription Fetal Lung lung
10 chr8:49619000-49626200 Weak transcription Spleen Spleen
11 chr8:49621000-49621400 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
12 chr8:49621000-49621600 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr8:49621000-49621600 Enhancers Skeletal Muscle Male skeletal muscle
14 chr8:49621000-49621600 Enhancers Skeletal Muscle Female skeletal muscle
15 chr8:49621000-49621800 Flanking Active TSS NHEK skin
16 chr8:49621200-49621400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr8:49621200-49621400 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
18 chr8:49621200-49621400 Enhancers Brain Germinal Matrix brain
19 chr8:49621200-49621600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
20 chr8:49621200-49621600 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
21 chr8:49621200-49621600 Flanking Active TSS HMEC breast
22 chr8:49621200-49621800 Enhancers Ovary ovary
23 chr8:49621200-49622400 Enhancers Placenta Placenta

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