Variant report

Variant rs373887979
Chromosome Location chr9:116859382-116859383
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116854800-116859600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr9:116855400-116859800 Weak transcription Lung lung
3 chr9:116855400-116859800 Weak transcription Rectal Mucosa Donor 31 rectum
4 chr9:116856400-116859800 Weak transcription Brain Inferior Temporal Lobe brain
5 chr9:116857400-116859800 Weak transcription Rectal Mucosa Donor 29 rectum
6 chr9:116858200-116859400 Weak transcription Fetal Kidney kidney
7 chr9:116858200-116859800 Weak transcription Liver Liver
8 chr9:116858400-116859400 Weak transcription Duodenum Mucosa Duodenum
9 chr9:116858400-116860000 Transcr. at gene 5' and 3' Fetal Intestine Small intestine
10 chr9:116858600-116859600 Genic enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr9:116858600-116859600 Genic enhancers Pancreas Pancrea
12 chr9:116858800-116859400 Weak transcription Gastric stomach
13 chr9:116858800-116860200 Enhancers HepG2 liver
14 chr9:116858800-116862200 Active TSS Pancreatic Islets Pancreatic Islet
15 chr9:116859000-116859800 Transcr. at gene 5' and 3' Fetal Intestine Large intestine
16 chr9:116859200-116859600 Bivalent Enhancer Primary mononuclear cells fromperipheralblood Blood
17 chr9:116859200-116859800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
18 chr9:116859200-116859800 Enhancers Breast Myoepithelial Primary Cells Breast
19 chr9:116859200-116860000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
20 chr9:116859200-116860200 Bivalent Enhancer Primary T helper cells fromperipheralblood blood
21 chr9:116859200-116860200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
22 chr9:116859200-116860200 Bivalent Enhancer Brain Germinal Matrix brain
23 chr9:116859200-116860600 Bivalent Enhancer Fetal Muscle Leg muscle

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