Variant report

Variant rs531499074
Chromosome Location chr5:60147886-60147887
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:60141200-60148000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr5:60147600-60149200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
3 chr5:60147800-60148000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr5:60147800-60149000 Enhancers Fetal Intestine Small intestine
5 chr5:60147800-60149000 Enhancers Placenta Placenta
6 chr5:60147800-60149200 Enhancers Fetal Intestine Large intestine
7 chr5:60147800-60149600 Enhancers K562 blood

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