Variant report

Variant rs10101649
Chromosome Location chr8:43102951-43102952
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:43101800-43103000 Bivalent/Poised TSS NHEK skin
2 chr8:43102000-43103000 Bivalent/Poised TSS Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr8:43102000-43103000 Bivalent Enhancer Primary T helper cells PMA-I stimulated --
4 chr8:43102000-43103200 Bivalent Enhancer Primary B cells from peripheral blood blood
5 chr8:43102200-43103000 Active TSS Right Atrium heart
6 chr8:43102200-43103200 Bivalent/Poised TSS Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr8:43102800-43103000 Bivalent Enhancer Primary T helper memory cells from peripheral blood 1 blood
8 chr8:43102800-43103000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
9 chr8:43102800-43103000 Flanking Bivalent TSS/Enh A549 lung

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