Variant report

Variant rs368211664
Chromosome Location chr5:180052034-180052035
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:180040000-180061200 Weak transcription Gastric stomach
2 chr5:180046200-180071800 Weak transcription Liver Liver
3 chr5:180046400-180072200 Weak transcription Right Atrium heart
4 chr5:180046800-180059600 Weak transcription Pancreas Pancrea
5 chr5:180048800-180052200 Enhancers Placenta Placenta
6 chr5:180050000-180052800 Enhancers Adipose Nuclei Adipose
7 chr5:180050000-180052800 Enhancers Right Ventricle heart
8 chr5:180050600-180052200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr5:180050800-180052200 Enhancers Lung lung
10 chr5:180051000-180056800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
11 chr5:180051600-180052800 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
12 chr5:180051600-180053600 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
13 chr5:180051600-180054800 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
14 chr5:180051800-180053000 Genic enhancers Spleen Spleen
15 chr5:180051800-180053600 Weak transcription Fetal Muscle Leg muscle

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