Variant report

Variant rs146810389
Chromosome Location chr21:45706533-45706534
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr21:45706000-45706600 Bivalent Enhancer Placenta Amnion Placenta Amnion
5 chr21:45706000-45706800 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
6 chr21:45706000-45707200 Weak transcription Primary hematopoietic stem cells blood
7 chr21:45706000-45708000 Weak transcription Pancreas Pancrea
8 chr21:45706000-45714800 Weak transcription Right Atrium heart
9 chr21:45706200-45709200 Enhancers Primary T helper 17 cells PMA-I stimulated --
10 chr21:45706400-45706600 Bivalent Enhancer Fetal Intestine Small intestine
11 chr21:45706400-45706600 Bivalent Enhancer Placenta Placenta
12 chr21:45706400-45706800 Bivalent/Poised TSS iPS DF 19.11 Cell Line embryonic stem cell
13 chr21:45706400-45706800 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin02 Skin
14 chr21:45706400-45706800 Bivalent Enhancer Fetal Intestine Large intestine
15 chr21:45706400-45706800 Enhancers Lung lung

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