Variant report

Variant rs35674918
Chromosome Location chr1:245954922-245954923
allele A/C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:245932000-245966200 Weak transcription Primary T cells from cord blood blood
2 chr1:245949200-245961400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr1:245949200-245999600 Weak transcription Gastric stomach
4 chr1:245949800-245955000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
5 chr1:245951400-245955200 Enhancers Placenta Amnion Placenta Amnion
6 chr1:245951600-245955000 Enhancers Osteobl bone
7 chr1:245951600-245955600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr1:245952000-245970400 Weak transcription Aorta Aorta
9 chr1:245953000-245955200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr1:245953800-245955000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr1:245954400-245956600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr1:245954600-245955200 Enhancers K562 blood
13 chr1:245954600-245955400 Enhancers Fetal Heart heart
14 chr1:245954800-245955400 Enhancers Fetal Lung lung

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