Variant report

Variant rs566108675
Chromosome Location chr7:99573725-99573726
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:99567800-99578000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr7:99571400-99573800 Active TSS Liver Liver
3 chr7:99572600-99573800 Active TSS Pancreas Pancrea
4 chr7:99572800-99573800 Active TSS HepG2 liver
5 chr7:99572800-99574000 Active TSS Brain Substantia Nigra brain
6 chr7:99572800-99574200 Enhancers Brain Cingulate Gyrus brain
7 chr7:99573000-99573800 Active TSS Gastric stomach
8 chr7:99573000-99574200 Enhancers Brain Inferior Temporal Lobe brain
9 chr7:99573400-99573800 Flanking Active TSS Adipose Nuclei Adipose
10 chr7:99573400-99573800 Active TSS Brain Anterior Caudate brain
11 chr7:99573400-99574200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
12 chr7:99573400-99574400 Enhancers Fetal Intestine Small intestine
13 chr7:99573400-99574600 Enhancers Stomach Mucosa stomach
14 chr7:99573600-99573800 Enhancers Brain Hippocampus Middle brain
15 chr7:99573600-99573800 Weak transcription Duodenum Mucosa Duodenum
16 chr7:99573600-99573800 Enhancers Left Ventricle heart
17 chr7:99573600-99574000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
18 chr7:99573600-99574200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin

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