Variant report

Variant rs545573240
Chromosome Location chr17:18285954-18285955
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:18267200-18288200 Weak transcription Right Atrium heart
2 chr17:18281400-18286400 Weak transcription Gastric stomach
3 chr17:18283000-18288200 Enhancers Fetal Thymus thymus
4 chr17:18283400-18287000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
5 chr17:18283800-18286200 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr17:18283800-18289400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr17:18284000-18286200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr17:18284200-18286000 Strong transcription Esophagus oesophagus
9 chr17:18285400-18286400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
10 chr17:18285800-18286000 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
11 chr17:18285800-18287000 Bivalent Enhancer Primary T cells fromperipheralblood blood

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