Variant report

Variant rs926455
Chromosome Location chr6:15876962-15876963
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:15870600-15884200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr6:15872200-15879400 Weak transcription Fetal Intestine Small intestine
3 chr6:15872600-15879200 Weak transcription Adipose Nuclei Adipose
4 chr6:15873600-15879000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr6:15873600-15879400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr6:15875000-15879400 Weak transcription NHLF lung
7 chr6:15875000-15880000 Weak transcription Psoas Muscle Psoas
8 chr6:15875400-15877200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr6:15875600-15882400 Enhancers Primary monocytes fromperipheralblood blood
10 chr6:15875800-15878600 Enhancers Monocytes-CD14+_RO01746 blood
11 chr6:15876400-15877200 Enhancers NHDF-Ad bronchial
12 chr6:15876400-15882200 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr6:15876600-15877200 Enhancers HUVEC blood vessel
14 chr6:15876600-15879600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr6:15876600-15882000 Enhancers Primary hematopoietic stem cells blood
16 chr6:15876600-15882200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
17 chr6:15876800-15877200 Enhancers GM12878-XiMat blood
18 chr6:15876800-15879000 Weak transcription Primary B cells from peripheral blood blood
19 chr6:15876800-15879800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links