Variant report

Variant rs553495050
Chromosome Location chr8:3961076-3961077
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:3958600-3962200 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr8:3958600-3963800 Enhancers HepG2 liver
3 chr8:3958800-3962600 Enhancers Fetal Intestine Large intestine
4 chr8:3958800-3962600 Enhancers Fetal Intestine Small intestine
5 chr8:3959000-3961600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr8:3959600-3961400 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr8:3959600-3961400 Weak transcription Fetal Muscle Leg muscle
8 chr8:3959600-3961400 Weak transcription Gastric stomach
9 chr8:3959600-3961400 Weak transcription Pancreas Pancrea
10 chr8:3959600-3961800 Enhancers Liver Liver
11 chr8:3959800-3961200 Weak transcription Cortex derived primary cultured neurospheres brain
12 chr8:3960000-3961800 Enhancers Fetal Lung lung
13 chr8:3960200-3961400 Weak transcription Stomach Mucosa stomach
14 chr8:3960400-3961400 Weak transcription Duodenum Mucosa Duodenum
15 chr8:3960400-3961800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
16 chr8:3960800-3961200 Weak transcription Rectal Mucosa Donor 31 rectum
17 chr8:3961000-3962000 Enhancers Adipose Nuclei Adipose

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