Variant report

Variant	rs4378971
Chromosome Location	chr3:68363844-68363845
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10155009	0.94[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap]
rs1397251	0.82[CHB][hapmap]
rs1491743	1.00[CHB][hapmap]
rs1491756	0.94[CEU][hapmap];1.00[CHB][hapmap]
rs1491757	0.94[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap]
rs169023	1.00[CHB][hapmap]
rs187794	1.00[CHB][hapmap]
rs262232	1.00[CHB][hapmap]
rs4345072	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap]
rs6549115	0.94[CEU][hapmap];0.87[YRI][hapmap]
rs6549116	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs6770136	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs6783358	1.00[CHB][hapmap]
rs7614996	1.00[CHB][hapmap]

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	esv2752014	chr3:68091879-68416989	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv1010992	chr3:68353191-68388825	Weak transcription Enhancers	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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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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