Variant report

Variant	rs1383815
Chromosome Location	chr8:51350639-51350640
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10808829	0.82[CHB][hapmap];0.81[ASN][1000 genomes]
rs10957910	1.00[CEU][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10957914	1.00[CHB][hapmap];0.84[JPT][hapmap];0.99[ASN][1000 genomes]
rs10957927	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1114500	0.82[CHB][hapmap]
rs1114808	0.82[CHB][hapmap]
rs11781401	0.82[CHB][hapmap]
rs11785117	0.86[ASW][hapmap]
rs12546744	0.88[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs13258865	0.82[CHB][hapmap]
rs1481467	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1481468	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1481482	0.82[CHB][hapmap]
rs1483643	0.82[CHB][hapmap]
rs1483644	0.82[CHB][hapmap]
rs1904997	0.82[CHB][hapmap]
rs1994031	0.82[CHB][hapmap]
rs2128000	0.82[CHB][hapmap]
rs2170373	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2251415	0.82[CHB][hapmap]
rs2448941	0.82[CHB][hapmap]
rs2467205	0.82[CHB][hapmap]
rs2623225	0.82[CHB][hapmap]
rs2625733	0.86[ASW][hapmap]
rs2625736	0.82[CHB][hapmap]
rs310558	0.82[CHB][hapmap]
rs4442158	0.82[CHB][hapmap]
rs4873459	0.82[CHB][hapmap];0.80[JPT][hapmap];0.82[ASN][1000 genomes]
rs6997739	1.00[ASW][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.84[GIH][hapmap];0.93[LWK][hapmap];0.91[MEX][hapmap];0.85[MKK][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7009024	0.84[TSI][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7827319	0.82[CHB][hapmap]
rs7839067	0.82[CHB][hapmap]
rs996524	0.82[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916392	chr8:50827638-51395140	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv948436	chr8:51115028-51917504	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv831312	chr8:51239772-51422844	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv916262	chr8:51322341-51437077	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51348400-51356200	Weak transcription	Fetal Intestine Small	intestine
2	chr8:51350600-51350800	Enhancers	Brain Germinal Matrix	brain
3	chr8:51350600-51351400	Flanking Active TSS	Liver	Liver
4	chr8:51350600-51351600	Enhancers	Fetal Intestine Large	intestine

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