Variant report

Variant rs16822344
Chromosome Location chr2:182884657-182884658
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:182843400-182904000 Weak transcription Thymus Thymus
2 chr2:182879800-182885000 Weak transcription Fetal Thymus thymus
3 chr2:182880800-182884800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
4 chr2:182880800-182885400 Weak transcription Stomach Mucosa stomach
5 chr2:182883000-182886000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr2:182883000-182886800 Enhancers Hela-S3 cervix
7 chr2:182883400-182884800 Enhancers NHLF lung
8 chr2:182883400-182885000 Weak transcription Muscle Satellite Cultured Cells --
9 chr2:182883400-182885200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr2:182883400-182885200 Weak transcription NHEK skin
11 chr2:182883600-182884800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr2:182883600-182885000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr2:182883600-182885000 Weak transcription Osteobl bone
14 chr2:182883600-182885200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr2:182883600-182885200 Weak transcription HMEC breast
16 chr2:182883600-182885600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr2:182884000-182886000 Enhancers Fetal Lung lung
18 chr2:182884400-182886800 Enhancers Dnd41 blood
19 chr2:182884600-182886000 Enhancers NH-A brain

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