Variant report

Variant rs4900616
Chromosome Location chr14:104775953-104775954
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:3 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104774800-104776000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr14:104775600-104776400 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
3 chr14:104775800-104776000 Enhancers Fetal Adrenal Gland Adrenal Gland

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