Variant report

Variant rs2797298
Chromosome Location chr6:380513-380514
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:376200-380600 Enhancers Primary B cells from cord blood blood
2 chr6:376400-381000 Enhancers Primary B cells from peripheral blood blood
3 chr6:378800-380600 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
4 chr6:379400-381000 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
5 chr6:379800-381600 Enhancers GM12878-XiMat blood
6 chr6:380200-380800 Bivalent/Poised TSS H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr6:380200-383600 Weak transcription Primary Natural Killer cells fromperipheralblood blood
8 chr6:380400-380800 Bivalent Enhancer Right Ventricle heart
9 chr6:380400-381000 ZNF genes & repeats Spleen Spleen

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