Variant report

Variant rs545217701
Chromosome Location chr1:172147637-172147638
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172123400-172149200 Weak transcription Brain Anterior Caudate brain
2 chr1:172128400-172149800 Weak transcription Aorta Aorta
3 chr1:172132800-172150000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
4 chr1:172138200-172147800 Weak transcription Brain Angular Gyrus brain
5 chr1:172138400-172149800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:172138600-172147800 Weak transcription Brain Hippocampus Middle brain
7 chr1:172138600-172147800 Weak transcription Brain Inferior Temporal Lobe brain
8 chr1:172139600-172148000 Weak transcription Fetal Stomach stomach
9 chr1:172142200-172149600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr1:172143600-172148000 Weak transcription Colon Smooth Muscle Colon
11 chr1:172145800-172150000 Weak transcription Psoas Muscle Psoas
12 chr1:172146000-172149000 Weak transcription Fetal Kidney kidney
13 chr1:172146400-172149600 Weak transcription Rectal Mucosa Donor 29 rectum
14 chr1:172146600-172150200 Enhancers Stomach Mucosa stomach
15 chr1:172146800-172148400 Enhancers Placenta Amnion Placenta Amnion
16 chr1:172146800-172152000 Enhancers Fetal Intestine Small intestine
17 chr1:172147200-172149000 Enhancers Fetal Lung lung
18 chr1:172147400-172154000 Weak transcription Sigmoid Colon Sigmoid Colon
19 chr1:172147600-172148000 Active TSS GM12878-XiMat blood
20 chr1:172147600-172149600 Enhancers Small Intestine intestine
21 chr1:172147600-172151200 Enhancers Fetal Intestine Large intestine

Quick Search:


  
Input of quick search could be:

what's new

Quick links