Variant report

Variant rs536899795
Chromosome Location chr14:68499758-68499759
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:68494800-68506200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr14:68495600-68500200 Weak transcription Pancreas Pancrea
3 chr14:68497400-68506200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr14:68498600-68500000 Enhancers Ovary ovary
5 chr14:68498800-68499800 Enhancers Fetal Intestine Small intestine
6 chr14:68498800-68500000 Enhancers Fetal Adrenal Gland Adrenal Gland
7 chr14:68498800-68503600 Enhancers Fetal Lung lung
8 chr14:68499200-68499800 Enhancers Colon Smooth Muscle Colon
9 chr14:68499400-68502200 Weak transcription Stomach Smooth Muscle stomach
10 chr14:68499400-68508400 Weak transcription Fetal Kidney kidney
11 chr14:68499600-68499800 Enhancers Primary hematopoietic stem cells blood
12 chr14:68499600-68499800 Enhancers Adipose Nuclei Adipose
13 chr14:68499600-68503200 Enhancers Rectal Smooth Muscle rectum

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