Variant report

Variant rs142873656
Chromosome Location chr1:71138506-71138507
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:71132800-71141000 Weak transcription Gastric stomach
2 chr1:71133800-71138600 Weak transcription Aorta Aorta
3 chr1:71134000-71140600 Weak transcription Pancreas Pancrea
4 chr1:71136200-71140400 Weak transcription Fetal Heart heart
5 chr1:71136800-71138800 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr1:71137000-71139200 Weak transcription K562 blood
7 chr1:71137000-71140600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr1:71137200-71140600 Weak transcription iPS-18 Cell Line embryonic stem cell
9 chr1:71137400-71139000 Enhancers Fetal Brain Female brain
10 chr1:71137400-71140600 Weak transcription Adipose Nuclei Adipose
11 chr1:71137600-71138600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr1:71137600-71139000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr1:71137600-71139200 Enhancers Fetal Lung lung
14 chr1:71137800-71138600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr1:71137800-71138600 Weak transcription Fetal Muscle Leg muscle
16 chr1:71137800-71138600 Weak transcription Fetal Stomach stomach
17 chr1:71138000-71138800 Enhancers Colon Smooth Muscle Colon
18 chr1:71138200-71138800 Enhancers Fetal Brain Male brain
19 chr1:71138400-71139400 Enhancers Ovary ovary

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