Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11751066	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11752582	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16884731	0.81[ASN][1000 genomes]
rs16884733	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16884746	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16884854	0.90[EUR][1000 genomes]
rs1830595	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3846756	0.83[ASN][1000 genomes]
rs41367946	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4385272	0.83[ASN][1000 genomes]
rs4441922	0.83[ASN][1000 genomes]
rs55766784	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs56168999	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56206543	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs71555263	1.00[AFR][1000 genomes]
rs72958951	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72958964	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72960912	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72960934	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72969239	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72969247	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72969251	0.84[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	esv2759442	chr6:74961996-75162222	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv35015	chr6:75031337-75154143	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2757178	chr6:75060947-75162222	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv886166	chr6:75082067-75155303	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv886167	chr6:75102625-75175449	Enhancers Weak transcription Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv886168	chr6:75112715-75166715	Enhancers Weak transcription Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75129800-75130600	Enhancers	Small Intestine	intestine
2	chr6:75129800-75131000	Enhancers	Fetal Intestine Large	intestine
3	chr6:75129800-75131200	Enhancers	Fetal Intestine Small	intestine
4	chr6:75130000-75130600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:75130000-75131000	Enhancers	Duodenum Mucosa	Duodenum
6	chr6:75130200-75130800	Enhancers	Stomach Mucosa	stomach

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