Variant report

Variant rs4819079
Chromosome Location chr21:46793801-46793802
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46782400-46798400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr21:46787600-46794000 Weak transcription Right Ventricle heart
3 chr21:46787600-46806800 Weak transcription Right Atrium heart
4 chr21:46787800-46796400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr21:46788000-46796400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr21:46788800-46794200 Weak transcription Adipose Nuclei Adipose
7 chr21:46792000-46794000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr21:46792000-46794000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr21:46792200-46794000 Enhancers HMEC breast
10 chr21:46792600-46794200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr21:46793000-46795200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
12 chr21:46793000-46795400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr21:46793400-46794200 Active TSS Spleen Spleen
14 chr21:46793400-46797600 Weak transcription K562 blood
15 chr21:46793400-46806400 Weak transcription Esophagus oesophagus
16 chr21:46793600-46794000 Weak transcription iPS-15b Cell Line embryonic stem cell
17 chr21:46793600-46794200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
18 chr21:46793800-46794000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
19 chr21:46793800-46794200 Bivalent Enhancer Placenta Placenta
20 chr21:46793800-46795000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
21 chr21:46793800-46798000 Weak transcription NH-A brain

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