Variant report

Variant rs57716863
Chromosome Location chr19:51433398-51433399
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:51429800-51433400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr19:51429800-51433400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr19:51430400-51435200 Weak transcription Hela-S3 cervix
4 chr19:51432400-51433400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr19:51432800-51433600 Enhancers Brain Hippocampus Middle brain
6 chr19:51432800-51435400 Weak transcription Esophagus oesophagus
7 chr19:51432800-51437400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr19:51433200-51433400 Bivalent Enhancer Primary T cells fromperipheralblood blood
9 chr19:51433200-51433400 Bivalent Enhancer Stomach Smooth Muscle stomach
10 chr19:51433200-51433600 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
11 chr19:51433200-51433600 Bivalent Enhancer Primary T helper cells PMA-I stimulated --
12 chr19:51433200-51433600 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
13 chr19:51433200-51433600 Enhancers A549 lung
14 chr19:51433200-51433800 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
15 chr19:51433200-51434000 Enhancers NHEK skin
16 chr19:51433200-51437600 Enhancers HMEC breast

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