Variant report

Variant rs2262371
Chromosome Location chr1:180289101-180289102
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:180257600-180289600 Weak transcription Hela-S3 cervix
2 chr1:180257800-180296200 Weak transcription Left Ventricle heart
3 chr1:180278000-180298200 Weak transcription Esophagus oesophagus
4 chr1:180278800-180296000 Weak transcription Pancreas Pancrea
5 chr1:180279000-180297600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr1:180279400-180295400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr1:180279600-180298800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr1:180281000-180295000 Weak transcription Fetal Stomach stomach
9 chr1:180281000-180295200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr1:180281000-180329400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr1:180282800-180295400 Weak transcription Primary B cells from cord blood blood
12 chr1:180282800-180313400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:180283000-180295000 Weak transcription Primary hematopoietic stem cells short term culture blood
14 chr1:180283000-180302800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
15 chr1:180283000-180302800 Weak transcription Fetal Intestine Large intestine

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