Variant report

Variant rs7020435
Chromosome Location chr9:18686448-18686449
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18667600-18690800 Weak transcription Aorta Aorta
2 chr9:18675600-18688800 Weak transcription HUVEC blood vessel
3 chr9:18675600-18695000 Weak transcription NHLF lung
4 chr9:18675800-18710000 Strong transcription HSMM muscle
5 chr9:18676200-18690800 Weak transcription Fetal Heart heart
6 chr9:18676800-18692000 Weak transcription HSMMtube muscle
7 chr9:18679800-18686600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr9:18679800-18689600 Strong transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:18680000-18701600 Strong transcription Osteobl bone
10 chr9:18680600-18693000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
11 chr9:18681400-18688000 Strong transcription NHDF-Ad bronchial
12 chr9:18683600-18686600 Enhancers Rectal Smooth Muscle rectum
13 chr9:18683800-18690600 Weak transcription Fetal Muscle Trunk muscle
14 chr9:18684000-18694600 Strong transcription NH-A brain
15 chr9:18684600-18689200 Strong transcription Muscle Satellite Cultured Cells --
16 chr9:18685000-18687200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr9:18685000-18687800 Strong transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
18 chr9:18685200-18694000 Weak transcription Fetal Stomach stomach
19 chr9:18685400-18687400 Weak transcription Fetal Lung lung
20 chr9:18685400-18689600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links