Variant report

Variant rs553405865
Chromosome Location chr5:94976982-94976983
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:94968200-94979800 Weak transcription Primary T cells from cord blood blood
2 chr5:94974800-94979800 Weak transcription GM12878-XiMat blood
3 chr5:94975200-94979200 Enhancers Pancreas Pancrea
4 chr5:94975600-94977400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr5:94976000-94982400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr5:94976600-94977000 Enhancers Right Atrium heart
7 chr5:94976600-94977400 Enhancers HepG2 liver
8 chr5:94976600-94978200 Enhancers Fetal Intestine Small intestine
9 chr5:94976600-94978600 Enhancers Fetal Intestine Large intestine
10 chr5:94976800-94977400 Weak transcription Gastric stomach
11 chr5:94976800-94978200 Enhancers Stomach Mucosa stomach
12 chr5:94976800-94978400 Enhancers Pancreatic Islets Pancreatic Islet
13 chr5:94976800-94982200 Enhancers Liver Liver

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