Variant report

Variant rs73180999
Chromosome Location chr7:100976244-100976245
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:100973600-100980600 Weak transcription Right Atrium heart
2 chr7:100973800-100977400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr7:100975600-100976400 Enhancers HepG2 liver
4 chr7:100976000-100976400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr7:100976000-100976600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr7:100976000-100976800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr7:100976200-100976600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr7:100976200-100976600 Enhancers Fetal Kidney kidney
9 chr7:100976200-100976800 Enhancers NHEK skin

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