Variant report

Variant rs73261983
Chromosome Location chr7:13102662-13102663
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:13095000-13103800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr7:13100400-13104000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr7:13101200-13103000 Enhancers Fetal Intestine Large intestine
4 chr7:13101400-13103600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr7:13101800-13102800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr7:13101800-13103000 Enhancers Fetal Intestine Small intestine
7 chr7:13102400-13102800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr7:13102400-13103000 Enhancers HepG2 liver
9 chr7:13102600-13102800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

Quick Search:


  
Input of quick search could be:

what's new

Quick links