Variant report

Variant rs1401132
Chromosome Location chr2:181891126-181891127
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:181856800-181897200 Weak transcription Primary B cells from cord blood blood
2 chr2:181857800-181901200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr2:181860000-181894800 Weak transcription Primary hematopoietic stem cells blood
4 chr2:181873400-181901000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:181886000-181901200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr2:181890200-181895600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr2:181890800-181901200 Weak transcription Primary T helper cells PMA-I stimulated --
8 chr2:181891000-181891200 Enhancers HUES64 Cell Line embryonic stem cell

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