Variant report

Variant rs187196036
Chromosome Location chr3:78890567-78890568
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:78882000-78894800 Weak transcription Fetal Intestine Small intestine
2 chr3:78886200-78895800 Weak transcription NHLF lung
3 chr3:78887200-78893000 Enhancers HepG2 liver
4 chr3:78887800-78896000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr3:78889000-78894800 Weak transcription Fetal Lung lung
6 chr3:78889200-78890600 Enhancers Brain Anterior Caudate brain
7 chr3:78889400-78896000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr3:78889400-78898800 Weak transcription Brain Inferior Temporal Lobe brain
9 chr3:78889400-78899000 Weak transcription Brain Hippocampus Middle brain
10 chr3:78889600-78896200 Weak transcription A549 lung
11 chr3:78889800-78895800 Weak transcription Brain Substantia Nigra brain
12 chr3:78890400-78890800 Enhancers Fetal Adrenal Gland Adrenal Gland
13 chr3:78890400-78891000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

Quick Search:


  
Input of quick search could be:

what's new

Quick links