Variant report

Variant rs16878127
Chromosome Location chr5:59771996-59771997
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:59741800-59783200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr5:59752400-59778400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr5:59767200-59789000 Weak transcription Primary B cells from cord blood blood
4 chr5:59770600-59772400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr5:59770600-59774800 Weak transcription Aorta Aorta
6 chr5:59770800-59773400 Weak transcription H1 Cell Line embryonic stem cell
7 chr5:59770800-59774400 Weak transcription H9 Cell Line embryonic stem cell
8 chr5:59771000-59773600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr5:59771400-59775200 Weak transcription HepG2 liver
10 chr5:59771600-59772600 Enhancers Fetal Brain Male brain

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