Variant report

Variant rs61827996
Chromosome Location chr1:170276255-170276256
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:170270400-170279200 Weak transcription Aorta Aorta
2 chr1:170271800-170278600 Weak transcription Right Atrium heart
3 chr1:170273200-170276800 Weak transcription NH-A brain
4 chr1:170273200-170278600 Weak transcription Ovary ovary
5 chr1:170275000-170277800 Enhancers NHLF lung
6 chr1:170275000-170278400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr1:170275200-170277200 Enhancers Osteobl bone
8 chr1:170275200-170277400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr1:170275400-170277200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr1:170275400-170278400 Weak transcription Fetal Muscle Leg muscle
11 chr1:170275400-170279000 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr1:170275600-170276400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr1:170275600-170277400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr1:170275600-170279000 Enhancers NHDF-Ad bronchial
15 chr1:170276000-170279200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr1:170276200-170278600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
17 chr1:170276200-170280400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived

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