Variant report

Variant rs4873606
Chromosome Location chr8:52717488-52717489
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:52708600-52721800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr8:52714400-52731800 Weak transcription Thymus Thymus
3 chr8:52715800-52722600 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr8:52716400-52721600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
5 chr8:52716400-52721600 Weak transcription Fetal Stomach stomach
6 chr8:52716600-52721200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr8:52716600-52728400 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr8:52717200-52717600 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
9 chr8:52717200-52717600 Enhancers Right Ventricle heart
10 chr8:52717200-52717800 Enhancers Adipose Nuclei Adipose
11 chr8:52717200-52717800 Genic enhancers Left Ventricle heart
12 chr8:52717400-52717600 ZNF genes & repeats Aorta Aorta
13 chr8:52717400-52717600 Enhancers Sigmoid Colon Sigmoid Colon
14 chr8:52717400-52717800 Enhancers Primary Natural Killer cells fromperipheralblood blood
15 chr8:52717400-52717800 Enhancers Lung lung
16 chr8:52717400-52717800 Enhancers Pancreas Pancrea
17 chr8:52717400-52717800 Enhancers Right Atrium heart
18 chr8:52717400-52717800 Enhancers Spleen Spleen

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