Variant report

Variant rs371293348
Chromosome Location chr2:180072650-180072651
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 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 chr2:180068000-180103800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr2:180068400-180092800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:180072400-180076800 Weak transcription Fetal Stomach stomach
6 chr2:180072400-180090400 Weak transcription Pancreas Pancrea

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