Variant report

Variant rs1392831
Chromosome Location chr10:1235018-1235019
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:1228200-1239000 Weak transcription Primary T cells from cord blood blood
2 chr10:1232200-1235600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
3 chr10:1232800-1239000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr10:1233000-1235600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr10:1233400-1236000 Enhancers Fetal Intestine Large intestine
6 chr10:1233600-1236600 Enhancers Brain Angular Gyrus brain
7 chr10:1234200-1236200 Enhancers Brain Anterior Caudate brain
8 chr10:1234200-1238000 Enhancers Brain Substantia Nigra brain
9 chr10:1234200-1238400 Enhancers Brain Hippocampus Middle brain
10 chr10:1234200-1241600 Enhancers Brain Inferior Temporal Lobe brain
11 chr10:1234400-1235200 Weak transcription Fetal Intestine Small intestine
12 chr10:1234400-1235400 Weak transcription Fetal Kidney kidney
13 chr10:1234400-1236200 Enhancers Brain Dorsolateral Prefrontal Cortex brain
14 chr10:1234600-1236000 Enhancers Pancreas Pancrea
15 chr10:1235000-1235200 Flanking Active TSS Brain Cingulate Gyrus brain

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