Variant report

Variant rs8129613
Chromosome Location chr21:46794769-46794770
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr21:46787600-46806800 Weak transcription Right Atrium heart
3 chr21:46787800-46796400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr21:46788000-46796400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr21:46793000-46795200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr21:46793000-46795400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr21:46793400-46797600 Weak transcription K562 blood
8 chr21:46793400-46806400 Weak transcription Esophagus oesophagus
9 chr21:46793800-46795000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr21:46793800-46798000 Weak transcription NH-A brain
11 chr21:46794000-46796800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
12 chr21:46794200-46794800 Weak transcription Spleen Spleen
13 chr21:46794200-46795000 Weak transcription Right Ventricle heart
14 chr21:46794200-46795200 Enhancers Adipose Nuclei Adipose
15 chr21:46794200-46796000 Enhancers Placenta Placenta
16 chr21:46794600-46795200 Bivalent Enhancer Fetal Muscle Trunk muscle

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