Variant report

Variant rs55872368
Chromosome Location chr1:159176856-159176857
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:159158800-159177600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr1:159158800-159177800 Weak transcription H9 Cell Line embryonic stem cell
3 chr1:159158800-159188800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr1:159168000-159177600 Weak transcription H1 Cell Line embryonic stem cell
5 chr1:159168400-159177600 Weak transcription Brain Angular Gyrus brain
6 chr1:159170400-159177800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr1:159170800-159177600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr1:159172600-159177200 Weak transcription Brain Germinal Matrix brain
9 chr1:159174800-159177200 Bivalent/Poised TSS Stomach Smooth Muscle stomach
10 chr1:159175200-159177800 Weak transcription HUES64 Cell Line embryonic stem cell
11 chr1:159175600-159177000 Enhancers Lung lung
12 chr1:159175800-159177600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
13 chr1:159176200-159177600 Weak transcription Placenta Placenta
14 chr1:159176200-159178200 Enhancers Spleen Spleen
15 chr1:159176600-159179200 Enhancers Fetal Brain Male brain
16 chr1:159176800-159177000 Enhancers Fetal Brain Female brain
17 chr1:159176800-159177000 Flanking Active TSS GM12878-XiMat blood

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