Variant report

Variant rs1006778
Chromosome Location chr21:46670989-46670990
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46669000-46672600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr21:46669000-46683400 Weak transcription H9 Cell Line embryonic stem cell
3 chr21:46669200-46672800 Weak transcription HUES6 Cell Line embryonic stem cell
4 chr21:46669200-46674600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr21:46669200-46677000 Weak transcription Left Ventricle heart
6 chr21:46669200-46706600 Weak transcription Right Atrium heart
7 chr21:46669400-46671000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr21:46669400-46671600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr21:46669400-46673200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr21:46669400-46673200 Weak transcription Osteobl bone
11 chr21:46670600-46671000 Enhancers Colon Smooth Muscle Colon
12 chr21:46670800-46671200 ZNF genes & repeats H1 Cell Line embryonic stem cell
13 chr21:46670800-46676200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --

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