Variant report

Variant rs73907152
Chromosome Location chr21:45706349-45706350
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:45702800-45714000 Weak transcription GM12878-XiMat blood
2 chr21:45703600-45707000 Bivalent Enhancer Fetal Muscle Trunk muscle
3 chr21:45704400-45711600 Weak transcription Primary B cells from cord blood blood
4 chr21:45705200-45706400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr21:45705800-45706400 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin01 Skin
6 chr21:45706000-45706400 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
7 chr21:45706000-45706600 Bivalent Enhancer Placenta Amnion Placenta Amnion
8 chr21:45706000-45706800 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
9 chr21:45706000-45707200 Weak transcription Primary hematopoietic stem cells blood
10 chr21:45706000-45708000 Weak transcription Pancreas Pancrea
11 chr21:45706000-45714800 Weak transcription Right Atrium heart
12 chr21:45706200-45706400 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
13 chr21:45706200-45706400 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
14 chr21:45706200-45709200 Enhancers Primary T helper 17 cells PMA-I stimulated --

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