Variant report

Variant rs1715175
Chromosome Location chr2:112027610-112027611
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:112008600-112048600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr2:112016600-112029000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr2:112019200-112032600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr2:112020600-112048000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr2:112022800-112031200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr2:112023400-112046400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr2:112025000-112034400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
8 chr2:112025400-112031000 Weak transcription Pancreas Pancrea
9 chr2:112025600-112116600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr2:112025800-112037800 Weak transcription HSMM muscle

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