Variant report

Variant rs2070526
Chromosome Location chr21:39971344-39971345
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:39967000-39971400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr21:39969000-39976600 Weak transcription H9 Cell Line embryonic stem cell
3 chr21:39969400-39973000 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr21:39970200-39977200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr21:39970400-39972000 Enhancers Spleen Spleen
6 chr21:39970400-39976600 Weak transcription Fetal Brain Male brain
7 chr21:39971000-39971600 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr21:39971200-39971800 Enhancers Adipose Nuclei Adipose
9 chr21:39971200-39972000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr21:39971200-39972400 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland

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