Variant report

Variant rs192177671
Chromosome Location chr19:52150361-52150362
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:52147200-52153400 Weak transcription Right Atrium heart
2 chr19:52149200-52150400 Weak transcription Spleen Spleen
3 chr19:52150200-52150400 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
4 chr19:52150200-52150400 Flanking Active TSS Primary monocytes fromperipheralblood blood
5 chr19:52150200-52150400 Flanking Active TSS Primary B cells from peripheral blood blood
6 chr19:52150200-52150400 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr19:52150200-52150400 Bivalent Enhancer Stomach Smooth Muscle stomach
8 chr19:52150200-52150600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr19:52150200-52150600 Flanking Active TSS Primary B cells from cord blood blood
10 chr19:52150200-52150600 Flanking Active TSS Primary hematopoietic stem cells short term culture blood
11 chr19:52150200-52150600 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr19:52150200-52150600 Bivalent Enhancer Adipose Nuclei Adipose
13 chr19:52150200-52150600 Active TSS Rectal Mucosa Donor 29 rectum
14 chr19:52150200-52150800 Flanking Active TSS Primary neutrophils fromperipheralblood blood
15 chr19:52150200-52150800 Enhancers Primary hematopoietic stem cells blood
16 chr19:52150200-52150800 Enhancers Primary Natural Killer cells fromperipheralblood blood
17 chr19:52150200-52150800 Enhancers GM12878-XiMat blood
18 chr19:52150200-52150800 Flanking Active TSS Monocytes-CD14+_RO01746 blood

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