Variant report

Variant	rs183878272
Chromosome Location	chr10:54042938-54042939
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:54040036..54043559-chr10:54043700..54046471,3	K562	blood:

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045692	chr10:53301450-54086823	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv532194	chr10:53746620-54735550	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv895399	chr10:53900872-54219820	Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv550889	chr10:54016062-54044615	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv825383	chr10:54041851-54043434	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54017400-54049600	Weak transcription	Left Ventricle	heart
2	chr10:54028000-54045600	Weak transcription	NHDF-Ad	bronchial
3	chr10:54029800-54055400	Weak transcription	Fetal Lung	lung
4	chr10:54032200-54044200	Weak transcription	Fetal Muscle Trunk	muscle
5	chr10:54036000-54050400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr10:54036800-54047400	Weak transcription	Fetal Intestine Large	intestine
7	chr10:54037800-54056000	Weak transcription	Fetal Muscle Leg	muscle
8	chr10:54040400-54044600	Weak transcription	Colon Smooth Muscle	Colon
9	chr10:54040600-54057000	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr10:54040800-54045400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr10:54041000-54048600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr10:54041400-54068200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr10:54042000-54043000	Enhancers	Psoas Muscle	Psoas
14	chr10:54042000-54043200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr10:54042000-54044600	Weak transcription	Adipose Nuclei	Adipose
16	chr10:54042400-54043200	Enhancers	HSMMtube	muscle
17	chr10:54042600-54043200	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr10:54042600-54043400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:54042800-54043000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
20	chr10:54042800-54043200	Genic enhancers	Skeletal Muscle Female	skeletal muscle
21	chr10:54042800-54068200	Weak transcription	Aorta	Aorta

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