Variant report

Variant rs2063002
Chromosome Location chr5:145567877-145567878
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:145562800-145569800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr5:145563000-145568000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr5:145563000-145568800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
4 chr5:145563000-145582200 Weak transcription Right Atrium heart
5 chr5:145563400-145570600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr5:145565200-145569800 Weak transcription HMEC breast
7 chr5:145565200-145570400 Weak transcription Osteobl bone
8 chr5:145567400-145568600 Enhancers NHEK skin
9 chr5:145567600-145570800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr5:145567600-145571000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr5:145567800-145568400 Enhancers NH-A brain
12 chr5:145567800-145568600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr5:145567800-145568600 Enhancers Muscle Satellite Cultured Cells --
14 chr5:145567800-145568600 Enhancers NHDF-Ad bronchial

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