Variant report

Variant rs72820904
Chromosome Location chr5:177740038-177740039
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177738200-177742200 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr5:177738800-177740200 Enhancers Esophagus oesophagus
3 chr5:177739000-177740800 Enhancers Primary monocytes fromperipheralblood blood
4 chr5:177739200-177740200 Enhancers H1 Cell Line embryonic stem cell
5 chr5:177739200-177740200 Enhancers HUES6 Cell Line embryonic stem cell
6 chr5:177739200-177740400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr5:177739400-177740200 Enhancers Stomach Mucosa stomach
8 chr5:177739400-177740400 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr5:177739600-177740200 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr5:177739600-177740400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
11 chr5:177739800-177740200 Enhancers ES-I3 Cell Line embryonic stem cell
12 chr5:177739800-177740400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
13 chr5:177739800-177741000 Enhancers Spleen Spleen
14 chr5:177739800-177747200 Weak transcription Fetal Lung lung
15 chr5:177739800-177757800 Weak transcription Gastric stomach
16 chr5:177740000-177740200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr5:177740000-177740400 Bivalent Enhancer Fetal Stomach stomach

Quick Search:


  
Input of quick search could be:

what's new

Quick links