Variant report

Variant rs559723166
Chromosome Location chr4:1106278-1106279
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:1104200-1107200 Weak transcription Rectal Mucosa Donor 31 rectum
2 chr4:1104400-1107000 Weak transcription A549 lung
3 chr4:1104600-1109600 Weak transcription Fetal Kidney kidney
4 chr4:1105600-1106400 Bivalent Enhancer Ganglion Eminence derived primary cultured neurospheres brain
5 chr4:1105600-1107200 Weak transcription HMEC breast
6 chr4:1105800-1106400 Bivalent Enhancer Brain Hippocampus Middle brain
7 chr4:1106000-1106400 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
8 chr4:1106000-1106400 Enhancers Brain Anterior Caudate brain
9 chr4:1106000-1106400 Flanking Active TSS Ovary ovary
10 chr4:1106000-1107200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr4:1106000-1108400 Active TSS Hela-S3 cervix
12 chr4:1106200-1106400 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
13 chr4:1106200-1106400 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
14 chr4:1106200-1106400 Flanking Bivalent TSS/Enh Fetal Muscle Trunk muscle
15 chr4:1106200-1106400 Flanking Active TSS Pancreas Pancrea
16 chr4:1106200-1106400 Enhancers Rectal Smooth Muscle rectum
17 chr4:1106200-1106400 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
18 chr4:1106200-1108200 Enhancers Primary B cells from peripheral blood blood

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