Variant report

Variant rs1298954
Chromosome Location chr1:145730160-145730161
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:145727200-145730600 Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr1:145727600-145730400 Active TSS Fetal Kidney kidney
3 chr1:145728200-145732000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr1:145728200-145738000 Weak transcription Pancreas Pancrea
5 chr1:145728400-145730400 Enhancers Pancreatic Islets Pancreatic Islet
6 chr1:145728800-145733600 Enhancers HepG2 liver
7 chr1:145729000-145730400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr1:145729000-145733400 Weak transcription Fetal Intestine Small intestine
9 chr1:145729200-145738600 Weak transcription Fetal Heart heart
10 chr1:145729400-145730400 Weak transcription Placenta Amnion Placenta Amnion
11 chr1:145729400-145731200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr1:145729400-145732600 Weak transcription Fetal Intestine Large intestine
13 chr1:145729400-145733200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr1:145729400-145733400 Enhancers Liver Liver

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