Variant report

Variant rs143794599
Chromosome Location chr17:18283024-18283025
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:18267200-18288200 Weak transcription Right Atrium heart
2 chr17:18280400-18284200 Enhancers Stomach Mucosa stomach
3 chr17:18280600-18283200 Enhancers Placenta Amnion Placenta Amnion
4 chr17:18280600-18283800 Enhancers Placenta Placenta
5 chr17:18281400-18286400 Weak transcription Gastric stomach
6 chr17:18281600-18283600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr17:18281600-18283800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr17:18281800-18283400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr17:18281800-18283600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr17:18282400-18283200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr17:18282600-18283800 Enhancers Esophagus oesophagus
12 chr17:18283000-18283200 Bivalent Enhancer Fetal Muscle Trunk muscle
13 chr17:18283000-18283800 Enhancers Rectal Mucosa Donor 29 rectum
14 chr17:18283000-18283800 Bivalent Enhancer NHEK skin
15 chr17:18283000-18288200 Enhancers Fetal Thymus thymus

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