Variant report

Variant rs201359421
Chromosome Location chr14:68500514-68500515
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr14:68497400-68506200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr14:68498800-68503600 Enhancers Fetal Lung lung
4 chr14:68499400-68502200 Weak transcription Stomach Smooth Muscle stomach
5 chr14:68499400-68508400 Weak transcription Fetal Kidney kidney
6 chr14:68499600-68503200 Enhancers Rectal Smooth Muscle rectum
7 chr14:68499800-68501600 Weak transcription Colon Smooth Muscle Colon
8 chr14:68499800-68501600 Weak transcription Fetal Intestine Small intestine
9 chr14:68499800-68512600 Weak transcription Adipose Nuclei Adipose
10 chr14:68499800-68516200 Weak transcription Primary hematopoietic stem cells blood
11 chr14:68500200-68500600 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr14:68500200-68500600 Enhancers Pancreas Pancrea
13 chr14:68500200-68501200 Enhancers Ovary ovary
14 chr14:68500400-68500600 Enhancers H9 Cell Line embryonic stem cell
15 chr14:68500400-68501200 Enhancers Right Atrium heart

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