Variant report

Variant rs58192162
Chromosome Location chr5:101491138-101491139
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:101488800-101491200 Active TSS ES-I3 Cell Line embryonic stem cell
2 chr5:101490000-101491200 Active TSS H9 Derived Neuron Cultured Cells ES cell derived
3 chr5:101490200-101491200 Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr5:101490200-101491200 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin01 Skin
5 chr5:101490200-101491200 Active TSS Primary mononuclear cells fromperipheralblood Blood
6 chr5:101490200-101491200 Active TSS Fetal Intestine Large intestine
7 chr5:101490200-101491200 Active TSS Fetal Intestine Small intestine
8 chr5:101490200-101491200 Active TSS Stomach Smooth Muscle stomach
9 chr5:101490400-101491200 Active TSS H1 Cell Line embryonic stem cell
10 chr5:101490400-101491200 Active TSS HUES6 Cell Line embryonic stem cell
11 chr5:101490400-101491200 Active TSS iPS-15b Cell Line embryonic stem cell
12 chr5:101490400-101491200 Active TSS Pancreas Pancrea
13 chr5:101490400-101491200 Active TSS Rectal Mucosa Donor 31 rectum
14 chr5:101490400-101491200 Active TSS Osteobl bone
15 chr5:101491000-101493600 Weak transcription Pancreatic Islets Pancreatic Islet

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