Variant report

Variant rs11144885
Chromosome Location chr9:79032157-79032158
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:79029600-79032800 Enhancers Stomach Mucosa stomach
2 chr9:79029800-79032600 Weak transcription H9 Cell Line embryonic stem cell
3 chr9:79030000-79032200 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr9:79030000-79032600 Weak transcription HUES64 Cell Line embryonic stem cell
5 chr9:79030400-79032600 Weak transcription H1 Cell Line embryonic stem cell
6 chr9:79030400-79038200 Weak transcription Fetal Adrenal Gland Adrenal Gland
7 chr9:79030800-79032200 Weak transcription HepG2 liver
8 chr9:79031000-79032200 Weak transcription Primary T cells from cord blood blood
9 chr9:79031000-79032200 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
10 chr9:79031000-79033000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
11 chr9:79031400-79032200 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
12 chr9:79031600-79034400 Weak transcription Pancreas Pancrea
13 chr9:79032000-79032200 Enhancers iPS-18 Cell Line embryonic stem cell
14 chr9:79032000-79032800 Enhancers iPS-15b Cell Line embryonic stem cell
15 chr9:79032000-79032800 Enhancers iPS-20b Cell Line embryonic stem cell

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