Variant report

Variant rs61062196
Chromosome Location chr2:234229926-234229927
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:234222200-234230200 Weak transcription GM12878-XiMat blood
2 chr2:234223600-234245400 Weak transcription Pancreas Pancrea
3 chr2:234228400-234240000 Weak transcription Fetal Intestine Small intestine
4 chr2:234228600-234231400 Enhancers Fetal Brain Male brain
5 chr2:234229600-234230000 Flanking Bivalent TSS/Enh HepG2 liver
6 chr2:234229800-234235000 Enhancers Primary B cells from cord blood blood
7 chr2:234229800-234235600 Enhancers Primary B cells from peripheral blood blood

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