Variant report

Variant rs55898668
Chromosome Location chr2:114601731-114601732
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 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 chr2:114596600-114603400 Weak transcription Primary T helper naive cells fromperipheralblood blood
4 chr2:114596600-114611600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
5 chr2:114596800-114632800 Weak transcription Primary T helper cells fromperipheralblood blood
6 chr2:114597600-114631400 Weak transcription Primary T helper cells PMA-I stimulated --
7 chr2:114600000-114601800 Enhancers Placenta Placenta
8 chr2:114600000-114602600 Weak transcription Primary T killer memory cells from peripheral blood blood
9 chr2:114600200-114602000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr2:114601200-114602000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr2:114601200-114602200 Enhancers HMEC breast
12 chr2:114601200-114606200 Weak transcription Fetal Adrenal Gland Adrenal Gland
13 chr2:114601200-114606800 Weak transcription NHLF lung
14 chr2:114601400-114601800 Enhancers NHEK skin
15 chr2:114601400-114602400 Enhancers NHDF-Ad bronchial
16 chr2:114601400-114602800 Enhancers Breast Myoepithelial Primary Cells Breast
17 chr2:114601400-114612000 Weak transcription Primary T cells from cord blood blood
18 chr2:114601600-114601800 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
19 chr2:114601600-114601800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
20 chr2:114601600-114601800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
21 chr2:114601600-114601800 Enhancers Osteobl bone
22 chr2:114601600-114606400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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