Variant report

Variant	rs184638308
Chromosome Location	chr21:28798993-28798994
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067475	chr21:28238746-29046707	Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv459229	chr21:28543456-29482488	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv587342	chr21:28543456-29482488	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv913666	chr21:28687650-28810976	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv916307	chr21:28762455-28905095	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv913667	chr21:28798703-28887357	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:28789400-28802000	Weak transcription	Left Ventricle	heart
2	chr21:28793800-28799000	Enhancers	NHDF-Ad	bronchial
3	chr21:28794000-28799200	Enhancers	Muscle Satellite Cultured Cells	--
4	chr21:28794200-28799000	Enhancers	HSMM	muscle
5	chr21:28795600-28801800	Weak transcription	Aorta	Aorta
6	chr21:28796600-28801800	Weak transcription	Fetal Stomach	stomach
7	chr21:28797800-28801800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr21:28798000-28801800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr21:28798200-28800600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr21:28798200-28801600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr21:28798200-28801800	Weak transcription	Right Ventricle	heart
12	chr21:28798400-28801800	Weak transcription	Ovary	ovary
13	chr21:28798400-28801800	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr21:28798600-28801800	Weak transcription	Adipose Nuclei	Adipose
15	chr21:28798600-28801800	Weak transcription	NHLF	lung
16	chr21:28798600-28801800	Weak transcription	Osteobl	bone
17	chr21:28798800-28801200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr21:28798800-28801600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr21:28798800-28801600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr21:28798800-28801800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr21:28798800-28801800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr21:28798800-28802000	Weak transcription	HSMMtube	muscle

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