Variant report

Variant rs72993556
Chromosome Location chr1:145731246-145731247
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:145728200-145732000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr1:145728200-145738000 Weak transcription Pancreas Pancrea
3 chr1:145728800-145733600 Enhancers HepG2 liver
4 chr1:145729000-145733400 Weak transcription Fetal Intestine Small intestine
5 chr1:145729200-145738600 Weak transcription Fetal Heart heart
6 chr1:145729400-145732600 Weak transcription Fetal Intestine Large intestine
7 chr1:145729400-145733200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
8 chr1:145729400-145733400 Enhancers Liver Liver
9 chr1:145730400-145733200 Weak transcription Fetal Kidney kidney
10 chr1:145730400-145742600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr1:145730600-145731800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr1:145731200-145731400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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