Variant report

Variant rs138775560
Chromosome Location chr17:18284121-18284122
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr17:18281400-18286400 Weak transcription Gastric stomach
4 chr17:18283000-18288200 Enhancers Fetal Thymus thymus
5 chr17:18283400-18287000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr17:18283800-18284200 Weak transcription Esophagus oesophagus
7 chr17:18283800-18284800 Weak transcription Rectal Mucosa Donor 29 rectum
8 chr17:18283800-18286200 Weak transcription HUES6 Cell Line embryonic stem cell
9 chr17:18283800-18289400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr17:18284000-18284200 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr17:18284000-18284200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
12 chr17:18284000-18284600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
13 chr17:18284000-18286200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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