Variant report

Variant rs10221749
Chromosome Location chr2:190159840-190159841
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:190152400-190162400 Weak transcription HMEC breast
2 chr2:190153600-190162800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr2:190153800-190162800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr2:190154800-190160200 Weak transcription Primary T killer memory cells from peripheral blood blood
5 chr2:190158400-190161600 Weak transcription HSMM muscle
6 chr2:190158400-190161800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr2:190158600-190161600 Weak transcription Muscle Satellite Cultured Cells --
8 chr2:190158600-190162600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr2:190158600-190162800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr2:190159000-190161600 Weak transcription Osteobl bone
11 chr2:190159000-190162600 Weak transcription NHDF-Ad bronchial
12 chr2:190159000-190162800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
13 chr2:190159600-190162000 Enhancers Primary T cells from cord blood blood
14 chr2:190159600-190162600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr2:190159800-190162800 Enhancers Primary T helper naive cells fromperipheralblood blood
16 chr2:190159800-190170800 Enhancers Primary T helper memory cells from peripheral blood 1 blood

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