Variant report

Variant rs2838903
Chromosome Location chr21:46805947-46805948
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46787600-46806800 Weak transcription Right Atrium heart
2 chr21:46793400-46806400 Weak transcription Esophagus oesophagus
3 chr21:46798200-46807600 Weak transcription H9 Cell Line embryonic stem cell
4 chr21:46802800-46808800 Bivalent Enhancer Fetal Muscle Trunk muscle
5 chr21:46803200-46807400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr21:46804200-46808400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr21:46804400-46808800 Enhancers Ovary ovary
8 chr21:46804800-46806600 Enhancers NHDF-Ad bronchial
9 chr21:46805000-46806000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr21:46805200-46806000 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
11 chr21:46805200-46806200 Weak transcription Fetal Muscle Leg muscle
12 chr21:46805200-46806400 Weak transcription Fetal Lung lung
13 chr21:46805400-46806600 Weak transcription Fetal Kidney kidney
14 chr21:46805400-46807600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr21:46805400-46808200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr21:46805800-46806000 Flanking Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
17 chr21:46805800-46806200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
18 chr21:46805800-46807400 Enhancers Pancreas Pancrea

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