Variant report

Variant rs2353
Chromosome Location chr1:147222372-147222373
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:147213400-147222400 Weak transcription Right Atrium heart
2 chr1:147219000-147224600 Weak transcription Placenta Placenta
3 chr1:147220000-147223200 Enhancers Hela-S3 cervix
4 chr1:147220200-147225200 Weak transcription Pancreas Pancrea
5 chr1:147220600-147222600 Enhancers NHEK skin
6 chr1:147220600-147223200 Enhancers HMEC breast
7 chr1:147220800-147228400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
8 chr1:147221000-147223600 Weak transcription Aorta Aorta
9 chr1:147221000-147224000 Enhancers Fetal Heart heart
10 chr1:147221200-147224800 Weak transcription Esophagus oesophagus
11 chr1:147221200-147228600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr1:147221400-147222400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr1:147221400-147222400 Weak transcription Left Ventricle heart
14 chr1:147221400-147224600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr1:147221400-147229000 Weak transcription Lung lung
16 chr1:147221600-147229600 Enhancers Breast Myoepithelial Primary Cells Breast
17 chr1:147222000-147223200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr1:147222000-147223400 Enhancers Right Ventricle heart
19 chr1:147222200-147223200 Enhancers Placenta Amnion Placenta Amnion

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