Variant report

Variant rs1094598
Chromosome Location chr1:180295065-180295066
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:180257800-180296200 Weak transcription Left Ventricle heart
2 chr1:180278000-180298200 Weak transcription Esophagus oesophagus
3 chr1:180278800-180296000 Weak transcription Pancreas Pancrea
4 chr1:180279000-180297600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr1:180279400-180295400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr1:180279600-180298800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr1:180281000-180295200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr1:180281000-180329400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr1:180282800-180295400 Weak transcription Primary B cells from cord blood blood
10 chr1:180282800-180313400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:180283000-180302800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr1:180283000-180302800 Weak transcription Fetal Intestine Large intestine
13 chr1:180293800-180296600 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr1:180294400-180303000 Weak transcription Placenta Placenta
15 chr1:180294600-180295600 Weak transcription Dnd41 blood
16 chr1:180294800-180296400 ZNF genes & repeats Fetal Intestine Small intestine
17 chr1:180295000-180296000 ZNF genes & repeats Primary T cells from cord blood blood
18 chr1:180295000-180296000 Strong transcription Fetal Stomach stomach
19 chr1:180295000-180296600 Strong transcription Primary hematopoietic stem cells short term culture blood

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