Variant report

Variant rs1934586
Chromosome Location chr1:245969321-245969322
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:245949200-245999600 Weak transcription Gastric stomach
2 chr1:245952000-245970400 Weak transcription Aorta Aorta
3 chr1:245955200-245970800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr1:245957000-245970400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr1:245961800-245980000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr1:245962000-245972600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr1:245962600-245970400 Weak transcription HepG2 liver
8 chr1:245963400-245970400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
9 chr1:245964600-245971200 Weak transcription Fetal Heart heart
10 chr1:245964800-245970400 Weak transcription NH-A brain
11 chr1:245964800-245973800 Weak transcription Fetal Stomach stomach
12 chr1:245966800-245970400 Weak transcription K562 blood
13 chr1:245968000-245970400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr1:245968200-245972600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
15 chr1:245968400-245975200 Weak transcription Placenta Placenta
16 chr1:245968400-245985800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
17 chr1:245968600-245969600 Enhancers Pancreatic Islets Pancreatic Islet

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