Variant report

Variant	rs1372220
Chromosome Location	chr5:111992382-111992383
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs17285372	0.82[EUR][1000 genomes]
rs17285666	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs17285827	0.82[EUR][1000 genomes]
rs17286230	0.82[EUR][1000 genomes]
rs17357294	0.82[EUR][1000 genomes]
rs17359859	1.00[CEU][hapmap]
rs17360045	1.00[CEU][hapmap]
rs56052440	0.82[EUR][1000 genomes]
rs56235416	0.82[EUR][1000 genomes]
rs73216225	0.82[EUR][1000 genomes]
rs7704566	0.82[EUR][1000 genomes]
rs7730944	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv599368	chr5:111399885-112032675	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv830450	chr5:111964170-112134510	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111976800-111992800	Weak transcription	Fetal Muscle Trunk	muscle
2	chr5:111984200-111993600	Weak transcription	Fetal Muscle Leg	muscle
3	chr5:111991000-111992400	Enhancers	Liver	Liver
4	chr5:111991400-111992800	Weak transcription	HSMMtube	muscle
5	chr5:111992200-111992600	Enhancers	HSMM	muscle

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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