Variant report

Variant rs534528907
Chromosome Location chr1:71138791-71138792
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:71132800-71141000 Weak transcription Gastric stomach
2 chr1:71134000-71140600 Weak transcription Pancreas Pancrea
3 chr1:71136200-71140400 Weak transcription Fetal Heart heart
4 chr1:71136800-71138800 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr1:71137000-71139200 Weak transcription K562 blood
6 chr1:71137000-71140600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr1:71137200-71140600 Weak transcription iPS-18 Cell Line embryonic stem cell
8 chr1:71137400-71139000 Enhancers Fetal Brain Female brain
9 chr1:71137400-71140600 Weak transcription Adipose Nuclei Adipose
10 chr1:71137600-71139000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr1:71137600-71139200 Enhancers Fetal Lung lung
12 chr1:71138000-71138800 Enhancers Colon Smooth Muscle Colon
13 chr1:71138200-71138800 Enhancers Fetal Brain Male brain
14 chr1:71138400-71139400 Enhancers Ovary ovary
15 chr1:71138600-71138800 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr1:71138600-71138800 Enhancers Aorta Aorta
17 chr1:71138600-71138800 Enhancers Fetal Stomach stomach
18 chr1:71138600-71139400 Enhancers Fetal Muscle Leg muscle

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