Variant report

Variant rs2996477
Chromosome Location chr1:92386234-92386235
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:92378400-92391400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr1:92379000-92389400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr1:92381600-92389800 Weak transcription HepG2 liver
4 chr1:92383600-92386600 Weak transcription Placenta Placenta
5 chr1:92383800-92386800 Weak transcription Placenta Amnion Placenta Amnion
6 chr1:92385800-92386600 Weak transcription Hela-S3 cervix
7 chr1:92386000-92393200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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