Variant report

Variant rs140327027
Chromosome Location chr5:180047588-180047589
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:180040000-180061200 Weak transcription Gastric stomach
2 chr5:180046000-180047600 Strong transcription Lung lung
3 chr5:180046000-180049600 Weak transcription Primary T killer naive cells fromperipheralblood blood
4 chr5:180046000-180050200 Weak transcription Primary T regulatory cells fromperipheralblood blood
5 chr5:180046200-180071800 Weak transcription Liver Liver
6 chr5:180046400-180049800 Weak transcription Primary T helper naive cells fromperipheralblood blood
7 chr5:180046400-180050000 Weak transcription Primary T cells from cord blood blood
8 chr5:180046400-180050600 Weak transcription Primary T helper cells fromperipheralblood blood
9 chr5:180046400-180051400 Weak transcription Primary hematopoietic stem cells blood
10 chr5:180046400-180072200 Weak transcription Right Atrium heart
11 chr5:180046600-180049200 Weak transcription Primary T helper cells PMA-I stimulated --
12 chr5:180046800-180047800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr5:180046800-180048800 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
14 chr5:180046800-180050200 Weak transcription Primary hematopoietic stem cells short term culture blood
15 chr5:180046800-180050600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
16 chr5:180046800-180059600 Weak transcription Pancreas Pancrea
17 chr5:180047000-180047800 Strong transcription Spleen Spleen
18 chr5:180047000-180048800 Bivalent Enhancer Placenta Placenta

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