Variant report

Variant rs12410041
Chromosome Location chr1:215286680-215286681
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:215281600-215287400 Weak transcription Cortex derived primary cultured neurospheres brain
2 chr1:215283400-215291200 Weak transcription Fetal Brain Female brain
3 chr1:215285400-215287000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr1:215285400-215287200 Enhancers Osteobl bone
5 chr1:215285400-215287800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:215285600-215286800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr1:215285600-215287000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:215285600-215287200 Weak transcription NHLF lung
9 chr1:215285800-215286800 Weak transcription HMEC breast
10 chr1:215286400-215287200 Enhancers Muscle Satellite Cultured Cells --
11 chr1:215286600-215287200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr1:215286600-215287200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
13 chr1:215286600-215287200 Enhancers HUVEC blood vessel
14 chr1:215286600-215287400 Enhancers NHDF-Ad bronchial
15 chr1:215286600-215289000 Enhancers Breast Myoepithelial Primary Cells Breast
16 chr1:215286600-215289000 Enhancers NHEK skin

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