Variant report

Variant rs16825505
Chromosome Location chr2:134234914-134234915
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:134231400-134240000 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr2:134232600-134236200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr2:134232600-134236200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr2:134232600-134236200 Enhancers HMEC breast
5 chr2:134232600-134236400 Enhancers NHEK skin
6 chr2:134232600-134236600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:134233400-134235200 Enhancers Fetal Intestine Large intestine
8 chr2:134234400-134235000 Enhancers Fetal Intestine Small intestine
9 chr2:134234600-134235200 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr2:134234600-134235400 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr2:134234800-134235000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
12 chr2:134234800-134235000 Enhancers Left Ventricle heart
13 chr2:134234800-134235200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr2:134234800-134235200 Enhancers Fetal Stomach stomach
15 chr2:134234800-134235200 Enhancers NHDF-Ad bronchial
16 chr2:134234800-134235600 Enhancers Ovary ovary

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