Variant report

Variant rs7573133
Chromosome Location chr2:114603501-114603502
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:114574200-114603600 Weak transcription Primary B cells from cord blood blood
2 chr2:114596400-114621000 Weak transcription Aorta Aorta
3 chr2:114596600-114611600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
4 chr2:114596800-114632800 Weak transcription Primary T helper cells fromperipheralblood blood
5 chr2:114597600-114631400 Weak transcription Primary T helper cells PMA-I stimulated --
6 chr2:114601200-114606200 Weak transcription Fetal Adrenal Gland Adrenal Gland
7 chr2:114601200-114606800 Weak transcription NHLF lung
8 chr2:114601400-114612000 Weak transcription Primary T cells from cord blood blood
9 chr2:114601600-114606400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr2:114601800-114604600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr2:114601800-114606200 Weak transcription NHEK skin
12 chr2:114601800-114606400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr2:114601800-114606400 Weak transcription Osteobl bone
14 chr2:114602000-114604600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr2:114602200-114604200 Weak transcription HMEC breast
16 chr2:114602400-114604000 Weak transcription NHDF-Ad bronchial
17 chr2:114602800-114626000 Weak transcription Breast Myoepithelial Primary Cells Breast
18 chr2:114603200-114603600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
19 chr2:114603400-114603800 Strong transcription Primary T helper naive cells fromperipheralblood blood

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