Variant report

Variant rs7045768
Chromosome Location chr9:21770709-21770710
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:21765400-21772600 Weak transcription HSMM muscle
2 chr9:21765600-21770800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr9:21767200-21771000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr9:21770200-21772000 Enhancers HMEC breast
5 chr9:21770400-21770800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr9:21770400-21771000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr9:21770400-21772000 Enhancers Hela-S3 cervix
8 chr9:21770400-21772800 Enhancers NHLF lung
9 chr9:21770400-21773400 Enhancers Stomach Mucosa stomach
10 chr9:21770600-21770800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr9:21770600-21771000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr9:21770600-21771000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr9:21770600-21771000 Enhancers Muscle Satellite Cultured Cells --
14 chr9:21770600-21771000 Enhancers NHDF-Ad bronchial
15 chr9:21770600-21771000 Enhancers NHEK skin
16 chr9:21770600-21771000 Enhancers Osteobl bone
17 chr9:21770600-21771400 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
18 chr9:21770600-21771800 Enhancers NH-A brain
19 chr9:21770600-21772000 Enhancers HUVEC blood vessel
20 chr9:21770600-21775800 Weak transcription Primary T helper cells PMA-I stimulated --

Quick Search:


  
Input of quick search could be:

what's new

Quick links