Variant report

Variant rs373052969
Chromosome Location chr12:7869327-7869328
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:7863400-7871000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr12:7864200-7870400 Weak transcription H1 Cell Line embryonic stem cell
3 chr12:7864200-7870400 Weak transcription H9 Cell Line embryonic stem cell
4 chr12:7864400-7870800 Weak transcription HUES6 Cell Line embryonic stem cell
5 chr12:7868200-7869800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr12:7868600-7869800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr12:7868800-7869400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr12:7869000-7869400 Enhancers HUES64 Cell Line embryonic stem cell
9 chr12:7869000-7869400 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr12:7869000-7869400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
11 chr12:7869000-7870400 Enhancers HUES48 Cell Line embryonic stem cell
12 chr12:7869200-7869400 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr12:7869200-7869600 Enhancers ES-I3 Cell Line embryonic stem cell
14 chr12:7869200-7869600 Enhancers iPS-18 Cell Line embryonic stem cell
15 chr12:7869200-7869600 Enhancers iPS-20b Cell Line embryonic stem cell

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