Variant report

Variant rs100659
Chromosome Location chr5:180039187-180039188
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:180018800-180045800 Weak transcription Right Atrium heart
2 chr5:180027800-180039600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr5:180028000-180039200 Weak transcription Lung lung
4 chr5:180029400-180045600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr5:180029800-180043200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr5:180033200-180039200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr5:180035600-180043400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
8 chr5:180037200-180041000 Weak transcription HUVEC blood vessel
9 chr5:180037200-180043200 Weak transcription Adipose Nuclei Adipose
10 chr5:180037400-180043400 Weak transcription Right Ventricle heart
11 chr5:180037600-180039200 Enhancers Placenta Placenta
12 chr5:180038800-180039200 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr5:180039000-180039400 Genic enhancers Spleen Spleen
14 chr5:180039000-180040000 Strong transcription Gastric stomach

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