Variant report

Variant rs372338892
Chromosome Location chrX:109636152-109636153
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:4 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:109626400-109638000 Weak transcription Placenta Amnion Placenta Amnion
2 chrX:109635000-109638200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chrX:109635800-109636400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chrX:109636000-109642200 Enhancers K562 blood

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