Variant report

Variant rs57988650
Chromosome Location chr10:22123983-22123984
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:22114200-22125000 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr10:22119600-22136800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr10:22121600-22138400 Weak transcription Primary B cells from cord blood blood
4 chr10:22122000-22124200 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr10:22122000-22124200 ZNF genes & repeats Fetal Stomach stomach
6 chr10:22123000-22124200 ZNF genes & repeats Fetal Intestine Small intestine
7 chr10:22123200-22124000 ZNF genes & repeats Primary Natural Killer cells fromperipheralblood blood
8 chr10:22123200-22124000 ZNF genes & repeats Gastric stomach
9 chr10:22123200-22124000 ZNF genes & repeats Left Ventricle heart
10 chr10:22123200-22124200 ZNF genes & repeats Duodenum Smooth Muscle Duodenum
11 chr10:22123200-22124200 ZNF genes & repeats Pancreas Pancrea
12 chr10:22123200-22125000 ZNF genes & repeats Liver Liver
13 chr10:22123200-22126000 Weak transcription Primary T helper cells PMA-I stimulated --
14 chr10:22123200-22138600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr10:22123600-22124000 ZNF genes & repeats Adipose Nuclei Adipose
16 chr10:22123800-22124200 ZNF genes & repeats Right Ventricle heart
17 chr10:22123800-22137600 Weak transcription Primary T cells from cord blood blood

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