Variant report

Variant rs1893632
Chromosome Location chr11:58599131-58599132
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:58596800-58604200 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr11:58597800-58599400 Weak transcription HMEC breast
3 chr11:58598000-58599600 Weak transcription Muscle Satellite Cultured Cells --
4 chr11:58598600-58599400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr11:58598600-58599800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr11:58598600-58600200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr11:58598600-58601200 Weak transcription HepG2 liver
8 chr11:58599000-58600000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr11:58599000-58600000 Enhancers NHEK skin

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