Variant report

Variant rs66587292
Chromosome Location chr7:19598681-19598682
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:19597200-19598800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr7:19597200-19599600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr7:19597200-19601400 Enhancers HMEC breast
4 chr7:19597400-19598800 Enhancers NHDF-Ad bronchial
5 chr7:19597400-19599200 Enhancers Osteobl bone
6 chr7:19597400-19600400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr7:19597400-19601400 Enhancers HSMMtube muscle
8 chr7:19597600-19601000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr7:19597800-19599000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr7:19597800-19599000 Enhancers NH-A brain
11 chr7:19597800-19599000 Enhancers NHEK skin
12 chr7:19597800-19599200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
13 chr7:19597800-19602000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr7:19598200-19599000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr7:19598200-19599000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
16 chr7:19598200-19599800 Weak transcription Skeletal Muscle Male skeletal muscle
17 chr7:19598200-19601600 Enhancers HSMM muscle
18 chr7:19598600-19598800 Flanking Active TSS Muscle Satellite Cultured Cells --

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