Variant report

Variant rs561881591
Chromosome Location chr7:99573506-99573507
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr7:99572400-99573600 Active TSS Pancreatic Islets Pancreatic Islet
4 chr7:99572400-99573600 Active TSS Right Ventricle heart
5 chr7:99572600-99573800 Active TSS Pancreas Pancrea
6 chr7:99572800-99573800 Active TSS HepG2 liver
7 chr7:99572800-99574000 Active TSS Brain Substantia Nigra brain
8 chr7:99572800-99574200 Enhancers Brain Cingulate Gyrus brain
9 chr7:99573000-99573600 Active TSS Duodenum Mucosa Duodenum
10 chr7:99573000-99573600 Active TSS Left Ventricle heart
11 chr7:99573000-99573800 Active TSS Gastric stomach
12 chr7:99573000-99574200 Enhancers Brain Inferior Temporal Lobe brain
13 chr7:99573400-99573800 Flanking Active TSS Adipose Nuclei Adipose
14 chr7:99573400-99573800 Active TSS Brain Anterior Caudate brain
15 chr7:99573400-99574200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
16 chr7:99573400-99574400 Enhancers Fetal Intestine Small intestine
17 chr7:99573400-99574600 Enhancers Stomach Mucosa stomach

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