Variant report

Variant rs193191445
Chromosome Location chr21:45706187-45706188
allele A/G
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 chr21:45703600-45706200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
3 chr21:45703600-45707000 Bivalent Enhancer Fetal Muscle Trunk muscle
4 chr21:45704400-45711600 Weak transcription Primary B cells from cord blood blood
5 chr21:45705200-45706200 Flanking Bivalent TSS/Enh iPS DF 19.11 Cell Line embryonic stem cell
6 chr21:45705200-45706200 Bivalent Enhancer Fetal Brain Male brain
7 chr21:45705200-45706400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr21:45705800-45706400 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin01 Skin
9 chr21:45706000-45706400 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
10 chr21:45706000-45706600 Bivalent Enhancer Placenta Amnion Placenta Amnion
11 chr21:45706000-45706800 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
12 chr21:45706000-45707200 Weak transcription Primary hematopoietic stem cells blood
13 chr21:45706000-45708000 Weak transcription Pancreas Pancrea
14 chr21:45706000-45714800 Weak transcription Right Atrium heart

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