Variant report

Variant rs371861902
Chromosome Location chr7:100334971-100334972
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:4 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:100319200-100342800 Weak transcription Right Atrium heart
2 chr7:100334400-100335000 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
3 chr7:100334800-100335000 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
4 chr7:100334800-100335000 Active TSS HepG2 liver

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