Variant report

Variant rs59629752
Chromosome Location chr2:191491274-191491275
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:191456600-191491800 Weak transcription Aorta Aorta
2 chr2:191475400-191492400 Weak transcription Fetal Brain Male brain
3 chr2:191477000-191491400 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr2:191486800-191492400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:191490000-191491800 Weak transcription HMEC breast
6 chr2:191490200-191492400 Enhancers NHDF-Ad bronchial
7 chr2:191490800-191492600 Weak transcription Psoas Muscle Psoas
8 chr2:191491200-191491400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr2:191491200-191491600 Enhancers Fetal Muscle Trunk muscle
10 chr2:191491200-191491800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr2:191491200-191491800 Enhancers Fetal Brain Female brain
12 chr2:191491200-191492000 Enhancers Right Ventricle heart
13 chr2:191491200-191492200 Enhancers Adipose Nuclei Adipose
14 chr2:191491200-191492200 Enhancers Brain Hippocampus Middle brain
15 chr2:191491200-191492400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
16 chr2:191491200-191492400 Enhancers Fetal Muscle Leg muscle
17 chr2:191491200-191492600 Enhancers Fetal Stomach stomach

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