Variant report

Variant rs72818491
Chromosome Location chr2:48536833-48536834
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:48506000-48539000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:48528000-48539200 Weak transcription Primary T cells from cord blood blood
3 chr2:48530200-48540200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr2:48533000-48539800 Weak transcription Primary B cells from cord blood blood
5 chr2:48534400-48538800 Weak transcription NHEK skin
6 chr2:48534400-48540200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr2:48534600-48539200 Weak transcription Hela-S3 cervix
8 chr2:48534600-48540200 Weak transcription Adipose Nuclei Adipose
9 chr2:48534600-48540200 Weak transcription NHDF-Ad bronchial
10 chr2:48534800-48539600 Weak transcription Placenta Placenta
11 chr2:48534800-48539600 Weak transcription Skeletal Muscle Male skeletal muscle
12 chr2:48534800-48539600 Weak transcription Skeletal Muscle Female skeletal muscle
13 chr2:48535000-48538400 Weak transcription HepG2 liver
14 chr2:48535600-48540400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
15 chr2:48535800-48539400 Weak transcription Primary T helper naive cells fromperipheralblood blood
16 chr2:48535800-48539600 Weak transcription Primary monocytes fromperipheralblood blood
17 chr2:48535800-48539600 Weak transcription Primary neutrophils fromperipheralblood blood
18 chr2:48536400-48539400 Weak transcription Primary T helper naive cells from peripheral blood blood

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