Variant report

Variant rs4899125
Chromosome Location chr14:39420235-39420236
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:39414200-39433600 Weak transcription Brain Angular Gyrus brain
2 chr14:39417800-39420400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr14:39417800-39420600 Weak transcription NH-A brain
4 chr14:39417800-39421000 Weak transcription Osteobl bone
5 chr14:39418000-39420400 Weak transcription Muscle Satellite Cultured Cells --
6 chr14:39418000-39420600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr14:39418000-39420600 Weak transcription HSMM muscle
8 chr14:39418000-39420800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr14:39418000-39428000 Weak transcription Brain Hippocampus Middle brain
10 chr14:39418400-39421000 Weak transcription Brain Substantia Nigra brain
11 chr14:39419800-39422400 Enhancers HUVEC blood vessel
12 chr14:39420000-39421800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr14:39420200-39420600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr14:39420200-39420800 Weak transcription HMEC breast
15 chr14:39420200-39420800 Weak transcription NHDF-Ad bronchial
16 chr14:39420200-39421000 Weak transcription Breast Myoepithelial Primary Cells Breast
17 chr14:39420200-39421200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links