Variant report

Variant rs372423435
Chromosome Location chr10:118999799-118999800
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:118997400-119000000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
2 chr10:118997600-119000200 Weak transcription Primary T cells from cord blood blood
3 chr10:118998200-119000000 Enhancers Primary hematopoietic stem cells blood
4 chr10:118998600-119000400 Enhancers Primary hematopoietic stem cells short term culture blood
5 chr10:118999000-119000200 Bivalent Enhancer Fetal Thymus thymus
6 chr10:118999000-119000600 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr10:118999400-118999800 Enhancers H1 Cell Line embryonic stem cell
8 chr10:118999400-119000000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr10:118999400-119000200 Bivalent Enhancer Ganglion Eminence derived primary cultured neurospheres brain
10 chr10:118999600-118999800 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
11 chr10:118999600-119000000 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
12 chr10:118999600-119000000 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
13 chr10:118999600-119000400 Flanking Active TSS iPS DF 19.11 Cell Line embryonic stem cell
14 chr10:118999600-119001800 Bivalent/Poised TSS iPS-20b Cell Line embryonic stem cell
15 chr10:118999600-119002000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell

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