Variant report

Variant rs532184079
Chromosome Location chr1:71444427-71444428
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:71441600-71444800 Enhancers Fetal Brain Male brain
2 chr1:71443200-71456800 Weak transcription Gastric stomach
3 chr1:71443600-71446000 Weak transcription Pancreas Pancrea
4 chr1:71444000-71444600 Enhancers Monocytes-CD14+_RO01746 blood
5 chr1:71444000-71445600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
6 chr1:71444200-71444600 Enhancers Fetal Heart heart
7 chr1:71444200-71446200 Enhancers Primary hematopoietic stem cells blood
8 chr1:71444200-71446600 Enhancers Adipose Nuclei Adipose
9 chr1:71444200-71447000 Enhancers Primary monocytes fromperipheralblood blood
10 chr1:71444400-71444600 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr1:71444400-71444800 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr1:71444400-71445400 Enhancers Cortex derived primary cultured neurospheres brain

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