Variant report

Variant rs9647229
Chromosome Location chr21:47154714-47154715
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47135600-47165000 Weak transcription Primary T cells from cord blood blood
2 chr21:47144200-47167600 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr21:47144600-47157600 Weak transcription Right Atrium heart
4 chr21:47145400-47156200 Weak transcription Brain Substantia Nigra brain
5 chr21:47146600-47159600 Weak transcription Spleen Spleen
6 chr21:47146600-47160000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr21:47151200-47155400 Weak transcription Primary neutrophils fromperipheralblood blood
8 chr21:47151800-47164800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
9 chr21:47152600-47157600 Strong transcription Fetal Thymus thymus
10 chr21:47152600-47160400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr21:47153200-47165400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr21:47154000-47154800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr21:47154000-47155000 Enhancers Fetal Stomach stomach
14 chr21:47154000-47156600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
15 chr21:47154400-47158000 Strong transcription Thymus Thymus
16 chr21:47154400-47160000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr21:47154600-47154800 Bivalent Enhancer Skeletal Muscle Female skeletal muscle

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