Variant report

Variant rs9430012
Chromosome Location chr1:209900615-209900616
allele C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:209894400-209907400 Weak transcription Right Ventricle heart
2 chr1:209895200-209902400 Weak transcription Left Ventricle heart
3 chr1:209897600-209903400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:209897800-209906200 Weak transcription Ovary ovary
5 chr1:209898000-209902200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr1:209899600-209902400 Enhancers Brain Cingulate Gyrus brain
7 chr1:209899800-209900800 Genic enhancers Liver Liver
8 chr1:209900000-209901200 Enhancers Brain Angular Gyrus brain
9 chr1:209900200-209901000 Enhancers Brain Inferior Temporal Lobe brain
10 chr1:209900200-209901200 Weak transcription Primary T helper cells PMA-I stimulated --
11 chr1:209900200-209901200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr1:209900200-209902600 Enhancers Brain Hippocampus Middle brain
13 chr1:209900400-209902000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr1:209900400-209902400 Enhancers Brain Substantia Nigra brain
15 chr1:209900600-209901000 Weak transcription Fetal Heart heart

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