Variant report

Variant rs184828766
Chromosome Location chr7:4999399-4999400
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:4998200-4999400 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
2 chr7:4998400-4999400 Bivalent/Poised TSS H1 Cell Line embryonic stem cell
3 chr7:4998400-4999400 Active TSS Ganglion Eminence derived primary cultured neurospheres brain
4 chr7:4998400-4999400 Active TSS Fetal Brain Female brain
5 chr7:4998400-4999400 Active TSS Right Ventricle heart
6 chr7:4998400-5002400 Weak transcription Fetal Brain Male brain
7 chr7:4998600-4999400 Active TSS H9 Cell Line embryonic stem cell
8 chr7:4998600-4999400 Active TSS iPS DF 6.9 Cell Line embryonic stem cell
9 chr7:4998600-4999400 Bivalent Enhancer Primary T helper cells PMA-I stimulated --
10 chr7:4998600-4999400 Active TSS Cortex derived primary cultured neurospheres brain
11 chr7:4998800-4999400 Active TSS ES-UCSF4 Cell Line embryonic stem cell
12 chr7:4999200-4999400 Flanking Bivalent TSS/Enh Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr7:4999200-4999400 Active TSS Brain Germinal Matrix brain
14 chr7:4999200-5000200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr7:4999200-5013400 Weak transcription Right Atrium heart

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