Variant report

Variant rs62220372
Chromosome Location chr21:45706738-45706739
allele C/T
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 chr21:45706000-45706800 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
5 chr21:45706000-45707200 Weak transcription Primary hematopoietic stem cells blood
6 chr21:45706000-45708000 Weak transcription Pancreas Pancrea
7 chr21:45706000-45714800 Weak transcription Right Atrium heart
8 chr21:45706200-45709200 Enhancers Primary T helper 17 cells PMA-I stimulated --
9 chr21:45706400-45706800 Bivalent/Poised TSS iPS DF 19.11 Cell Line embryonic stem cell
10 chr21:45706400-45706800 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin02 Skin
11 chr21:45706400-45706800 Bivalent Enhancer Fetal Intestine Large intestine
12 chr21:45706400-45706800 Enhancers Lung lung
13 chr21:45706600-45706800 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
14 chr21:45706600-45707000 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
15 chr21:45706600-45707600 Enhancers ES-UCSF4 Cell Line embryonic stem cell

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