Variant report

Variant rs531363157
Chromosome Location chr2:180071027-180071028
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180067600-180097600 Weak transcription Primary B cells from cord blood blood
2 chr2:180067600-180104600 Weak transcription Fetal Kidney kidney
3 chr2:180068000-180071400 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr2:180068000-180103800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr2:180068400-180092800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:180068600-180071200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr2:180068600-180071200 Weak transcription Fetal Stomach stomach
8 chr2:180070200-180071200 Weak transcription Adipose Nuclei Adipose
9 chr2:180070800-180071600 ZNF genes & repeats Fetal Intestine Small intestine
10 chr2:180071000-180071200 Enhancers Brain Inferior Temporal Lobe brain

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