Variant report

Variant rs26951
Chromosome Location chr5:59759657-59759658
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:59727200-59766600 Weak transcription Primary B cells from cord blood blood
2 chr5:59741800-59783200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr5:59749800-59760600 Weak transcription Aorta Aorta
4 chr5:59752400-59778400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr5:59758200-59768800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr5:59758400-59760000 Flanking Active TSS A549 lung
7 chr5:59758800-59759800 Enhancers Placenta Placenta
8 chr5:59759200-59759800 Enhancers Fetal Intestine Large intestine
9 chr5:59759200-59760600 Enhancers Placenta Amnion Placenta Amnion
10 chr5:59759200-59760600 Enhancers Stomach Smooth Muscle stomach
11 chr5:59759400-59759800 Enhancers Duodenum Smooth Muscle Duodenum
12 chr5:59759400-59760000 Enhancers Primary B cells from peripheral blood blood
13 chr5:59759600-59760400 Weak transcription Right Atrium heart
14 chr5:59759600-59760800 Enhancers HepG2 liver

Quick Search:


  
Input of quick search could be:

what's new

Quick links