Variant report

Variant rs7932168
Chromosome Location chr11:26617479-26617480
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:26600400-26643000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr11:26603800-26623200 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr11:26604000-26623600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr11:26607600-26635400 Weak transcription Adipose Nuclei Adipose
5 chr11:26610800-26619000 Weak transcription Fetal Lung lung
6 chr11:26616000-26617600 Enhancers Fetal Intestine Large intestine
7 chr11:26616000-26617600 Enhancers Fetal Intestine Small intestine
8 chr11:26616600-26617600 Enhancers Primary neutrophils fromperipheralblood blood

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