Variant report

Variant rs10015342
Chromosome Location chr4:74713799-74713800
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:74706600-74719000 Weak transcription Pancreas Pancrea
2 chr4:74710800-74718600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr4:74710800-74718800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr4:74711200-74718800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr4:74711400-74718800 Weak transcription HMEC breast
6 chr4:74712600-74715800 Enhancers Primary neutrophils fromperipheralblood blood
7 chr4:74713000-74714000 Enhancers Primary monocytes fromperipheralblood blood
8 chr4:74713000-74714000 Enhancers Monocytes-CD14+_RO01746 blood
9 chr4:74713200-74713800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr4:74713200-74714000 Enhancers Primary hematopoietic stem cells short term culture blood
11 chr4:74713200-74714000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr4:74713400-74713800 Enhancers Primary hematopoietic stem cells blood
13 chr4:74713400-74714200 Enhancers Primary B cells from cord blood blood
14 chr4:74713400-74715600 Enhancers Liver Liver
15 chr4:74713600-74713800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin

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