Variant report

Variant rs6904381
Chromosome Location chr6:119261916-119261917
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:119256600-119262000 Weak transcription Pancreas Pancrea
2 chr6:119256800-119262000 Weak transcription Thymus Thymus
3 chr6:119257000-119262400 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
4 chr6:119257400-119262000 Weak transcription Primary B cells from cord blood blood
5 chr6:119259600-119262400 Strong transcription Primary T cells from cord blood blood
6 chr6:119260800-119262000 ZNF genes & repeats Fetal Stomach stomach
7 chr6:119260800-119262200 Enhancers Left Ventricle heart
8 chr6:119260800-119262600 ZNF genes & repeats Fetal Intestine Small intestine
9 chr6:119261000-119268600 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr6:119261400-119262200 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
11 chr6:119261600-119262200 Enhancers Breast Myoepithelial Primary Cells Breast
12 chr6:119261600-119262400 Enhancers Primary B cells from peripheral blood blood
13 chr6:119261600-119262400 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr6:119261800-119262000 Enhancers Gastric stomach
15 chr6:119261800-119262000 Enhancers Right Atrium heart

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