Variant report

Variant rs563919646
Chromosome Location chr9:975783-975784
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:973000-976200 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
2 chr9:973200-976000 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
3 chr9:974000-976000 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
4 chr9:974400-977800 Bivalent Enhancer Primary monocytes fromperipheralblood blood
5 chr9:974800-976000 Bivalent Enhancer H9 Cell Line embryonic stem cell
6 chr9:974800-976000 Bivalent Enhancer Fetal Muscle Trunk muscle
7 chr9:975000-975800 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
8 chr9:975200-976000 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
9 chr9:975200-976800 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
10 chr9:975400-975800 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
11 chr9:975400-975800 Bivalent Enhancer H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr9:975400-975800 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
13 chr9:975400-976200 Weak transcription Pancreas Pancrea
14 chr9:975400-976200 Bivalent Enhancer Stomach Smooth Muscle stomach
15 chr9:975400-978800 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
16 chr9:975600-975800 Flanking Bivalent TSS/Enh hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
17 chr9:975600-975800 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
18 chr9:975600-976000 Bivalent Enhancer Adipose Nuclei Adipose
19 chr9:975600-976000 Bivalent Enhancer Colonic Mucosa Colon
20 chr9:975600-976400 Flanking Bivalent TSS/Enh H1 Cell Line embryonic stem cell
21 chr9:975600-977400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin

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