Variant report

Variant rs4959252
Chromosome Location chr6:420020-420021
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:3 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:412000-420800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr6:412200-422400 Weak transcription Primary T helper 17 cells PMA-I stimulated --
3 chr6:419800-420200 Enhancers Placenta Amnion Placenta Amnion

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