Variant report

Variant rs4908992
Chromosome Location chr3:17693974-17693975
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:17668800-17706200 Weak transcription Primary B cells from cord blood blood
2 chr3:17681800-17714400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr3:17687200-17694200 Weak transcription Brain Inferior Temporal Lobe brain
4 chr3:17687400-17694200 Weak transcription A549 lung
5 chr3:17689200-17704000 Weak transcription Primary B cells from peripheral blood blood
6 chr3:17693600-17697400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr3:17693600-17697600 Weak transcription Brain Substantia Nigra brain

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