Variant report

Variant rs11984531
Chromosome Location chr8:100281886-100281887
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:100207000-100290400 Weak transcription Primary T helper cells fromperipheralblood blood
2 chr8:100214800-100293200 Weak transcription Primary T cells fromperipheralblood blood
3 chr8:100246400-100288200 Weak transcription Primary T cells from cord blood blood
4 chr8:100253400-100292400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr8:100263600-100287800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr8:100268200-100293200 Weak transcription Aorta Aorta
7 chr8:100268400-100290000 Weak transcription Primary T helper cells PMA-I stimulated --
8 chr8:100273000-100290400 Weak transcription Primary T killer memory cells from peripheral blood blood
9 chr8:100274400-100292200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr8:100278800-100302400 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
11 chr8:100280600-100293200 Weak transcription Left Ventricle heart
12 chr8:100280800-100282400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr8:100280800-100292200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
14 chr8:100280800-100299000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
15 chr8:100281200-100283800 Weak transcription Primary B cells from cord blood blood

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