Variant report

Variant rs58358642
Chromosome Location chr5:43355168-43355169
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:43351200-43357200 Weak transcription Esophagus oesophagus
2 chr5:43351600-43356800 Weak transcription Fetal Intestine Large intestine
3 chr5:43351600-43356800 Weak transcription Fetal Intestine Small intestine
4 chr5:43353800-43355200 Enhancers NHEK skin
5 chr5:43353800-43355400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr5:43354000-43355200 Enhancers HMEC breast
7 chr5:43354400-43355200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr5:43354400-43357200 Weak transcription K562 blood
9 chr5:43354800-43355200 Enhancers Breast Myoepithelial Primary Cells Breast

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