Variant report

Variant rs6684466
Chromosome Location chr1:10069325-10069326
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:10059200-10075000 Weak transcription Fetal Heart heart
2 chr1:10061600-10077000 Weak transcription Brain Hippocampus Middle brain
3 chr1:10061800-10077200 Weak transcription Brain Substantia Nigra brain
4 chr1:10066600-10069800 Weak transcription Spleen Spleen
5 chr1:10066800-10071000 Weak transcription Adipose Nuclei Adipose
6 chr1:10067400-10070200 Strong transcription Primary monocytes fromperipheralblood blood
7 chr1:10067400-10070200 Strong transcription Monocytes-CD14+_RO01746 blood
8 chr1:10067800-10070000 Strong transcription Primary neutrophils fromperipheralblood blood
9 chr1:10068000-10075600 Weak transcription Left Ventricle heart

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