Variant report

Variant rs704731
Chromosome Location chr11:34687193-34687194
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:34674800-34689200 Weak transcription Gastric stomach
2 chr11:34676600-34689200 Weak transcription Esophagus oesophagus
3 chr11:34677000-34688800 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr11:34678200-34689600 Weak transcription Stomach Mucosa stomach
5 chr11:34681600-34689200 Weak transcription Pancreas Pancrea
6 chr11:34683400-34687200 Weak transcription Duodenum Mucosa Duodenum
7 chr11:34683800-34689600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr11:34686400-34689600 Enhancers HepG2 liver
9 chr11:34686600-34687400 Enhancers K562 blood
10 chr11:34686600-34687800 Enhancers Liver Liver
11 chr11:34686800-34687200 Flanking Active TSS A549 lung
12 chr11:34686800-34687600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr11:34686800-34687600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr11:34686800-34690000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
15 chr11:34687000-34687200 Enhancers Brain Hippocampus Middle brain
16 chr11:34687000-34687400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr11:34687000-34687400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
18 chr11:34687000-34687400 Flanking Active TSS NHEK skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links