Variant report

Variant rs575599371
Chromosome Location chr6:26698582-26698583
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:26697600-26698600 Active TSS ES-I3 Cell Line embryonic stem cell
2 chr6:26697600-26698600 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
3 chr6:26697600-26698600 Bivalent/Poised TSS iPS-20b Cell Line embryonic stem cell
4 chr6:26697600-26699000 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell
5 chr6:26697800-26698600 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
6 chr6:26697800-26698600 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
7 chr6:26698000-26698600 Bivalent/Poised TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr6:26698000-26698600 Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
9 chr6:26698000-26698800 Bivalent/Poised TSS Stomach Smooth Muscle stomach
10 chr6:26698000-26698800 Bivalent/Poised TSS NHEK skin
11 chr6:26698200-26698800 Bivalent/Poised TSS H1 Cell Line embryonic stem cell
12 chr6:26698200-26698800 Bivalent/Poised TSS Ganglion Eminence derived primary cultured neurospheres brain
13 chr6:26698200-26698800 Bivalent/Poised TSS Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr6:26698200-26698800 Bivalent/Poised TSS NHDF-Ad bronchial
15 chr6:26698400-26698600 Enhancers H9 Cell Line embryonic stem cell
16 chr6:26698400-26698600 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
17 chr6:26698400-26698600 Bivalent/Poised TSS Osteobl bone
18 chr6:26698400-26698800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
19 chr6:26698400-26698800 Enhancers HMEC breast
20 chr6:26698400-26701400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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