The 2.0 version of rSNPBase

Variant report

Variant rs13097562
Chromosome Location chr3:177430535-177430536
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:177413600-177432000 Weak transcription Primary hematopoietic stem cells blood
2 chr3:177422200-177431800 Weak transcription Aorta Aorta
3 chr3:177424600-177431400 Weak transcription Stomach Smooth Muscle stomach
4 chr3:177425000-177431600 Weak transcription Adipose Nuclei Adipose
5 chr3:177425600-177432000 Weak transcription Psoas Muscle Psoas
6 chr3:177426000-177431400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr3:177428800-177431400 Weak transcription Colon Smooth Muscle Colon
8 chr3:177429800-177431600 Weak transcription Primary hematopoietic stem cells short term culture blood
9 chr3:177429800-177431800 Weak transcription Fetal Thymus thymus
10 chr3:177429800-177432000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr3:177429800-177432000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr3:177429800-177432400 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr3:177430000-177432000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr3:177430000-177432000 Weak transcription NHEK skin
15 chr3:177430000-177448200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
16 chr3:177430000-177449000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr3:177430200-177431800 Weak transcription Skeletal Muscle Male skeletal muscle

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Last update: Aug 31, 2015