Variant report

Variant rs17166029
Chromosome Location chr7:12477055-12477056
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:12475800-12477200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
2 chr7:12476400-12477200 Enhancers HUES48 Cell Line embryonic stem cell
3 chr7:12476400-12477200 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr7:12476400-12477200 Enhancers Brain Germinal Matrix brain
5 chr7:12476600-12477200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
6 chr7:12476600-12477400 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr7:12476800-12477200 Enhancers HUES64 Cell Line embryonic stem cell
8 chr7:12476800-12477200 Flanking Active TSS NH-A brain
9 chr7:12476800-12478000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr7:12477000-12490000 Weak transcription ES-I3 Cell Line embryonic stem cell

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