Variant report

Variant rs189001
Chromosome Location chr1:210167034-210167035
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210159600-210168200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr1:210162800-210189200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:210166200-210167200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr1:210166200-210167200 Genic enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr1:210166600-210167400 Strong transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr1:210167000-210167200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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