Variant report

Variant	rs4730974
Chromosome Location	chr7:120312746-120312747
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10251949	1.00[JPT][hapmap]
rs10256493	1.00[JPT][hapmap]
rs10256716	1.00[JPT][hapmap]
rs10272339	1.00[JPT][hapmap]
rs10487403	1.00[JPT][hapmap]
rs17142902	1.00[JPT][hapmap]
rs17142974	1.00[JPT][hapmap]
rs1859534	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap]
rs41424845	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6466755	1.00[JPT][hapmap]
rs66922945	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66986475	0.90[EUR][1000 genomes]
rs67108130	0.91[EUR][1000 genomes]
rs67355198	0.85[EUR][1000 genomes]
rs67907055	0.82[EUR][1000 genomes]
rs7790895	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs7795370	1.00[JPT][hapmap]
rs7812111	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

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	esv2761361	chr7:120304367-120312759	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv2829884	chr7:120305149-120312746	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv517677	chr7:120305149-120312746	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv818550	chr7:120305149-120312746	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv524688	chr7:120305149-120327349	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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