Variant report

Variant	rs4144948
Chromosome Location	chr15:54532795-54532796
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10851559	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11634827	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12161946	0.83[EUR][1000 genomes]
rs16974322	0.80[EUR][1000 genomes]
rs16974341	0.83[EUR][1000 genomes]
rs16974346	0.85[EUR][1000 genomes]
rs16974347	0.85[EUR][1000 genomes]
rs16974350	0.85[EUR][1000 genomes]
rs16974352	0.85[EUR][1000 genomes]
rs16974354	0.84[EUR][1000 genomes]
rs16974357	0.84[EUR][1000 genomes]
rs28362165	0.84[EUR][1000 genomes]
rs28410351	0.85[EUR][1000 genomes]
rs28550623	0.85[EUR][1000 genomes]
rs28676923	0.85[EUR][1000 genomes]
rs28737427	0.83[EUR][1000 genomes]
rs60148245	0.80[EUR][1000 genomes]
rs60183354	0.80[EUR][1000 genomes]
rs7163335	0.80[EUR][1000 genomes]
rs7178272	0.81[EUR][1000 genomes]
rs73409976	0.80[EUR][1000 genomes]
rs73409977	0.80[EUR][1000 genomes]
rs73411912	0.85[EUR][1000 genomes]
rs73411926	0.85[EUR][1000 genomes]
rs74013519	0.83[EUR][1000 genomes]
rs8023764	0.82[EUR][1000 genomes]
rs8030340	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]

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	nsv1052235	chr15:53677524-54618723	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv542388	chr15:53677524-54618723	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv817539	chr15:54132584-55095235	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1043666	chr15:54415970-54548495	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1043823	chr15:54468477-54532985	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv12090	chr15:54532412-54533030	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54519000-54554400	Weak transcription	Aorta	Aorta
2	chr15:54519400-54549600	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr15:54531400-54544800	Weak transcription	Fetal Lung	lung

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