The 2.0 version of rSNPBase

Variant report

Variant rs10098392
Chromosome Location chr8:129888027-129888028
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:129881600-129894200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
2 chr8:129882800-129888600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr8:129886200-129891400 Enhancers Dnd41 blood
4 chr8:129887000-129888800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr8:129887000-129889400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr8:129887200-129889200 Weak transcription Fetal Stomach stomach
7 chr8:129887200-129894000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr8:129887400-129888400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
9 chr8:129887400-129888600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr8:129887400-129888600 Weak transcription NHDF-Ad bronchial
11 chr8:129887400-129889200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr8:129887400-129889400 Weak transcription Fetal Thymus thymus
13 chr8:129887400-129889800 Weak transcription Cortex derived primary cultured neurospheres brain
14 chr8:129887400-129894800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr8:129887400-129896000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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Last update: Aug 31, 2015