Variant report

Variant	rs10235982
Chromosome Location	chr7:19075743-19075744
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10216193	0.92[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10224508	1.00[ASN][1000 genomes]
rs10228000	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10228944	1.00[ASN][1000 genomes]
rs10229075	1.00[ASN][1000 genomes]
rs10229095	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10240640	0.92[EUR][1000 genomes]
rs10248134	1.00[EUR][1000 genomes]
rs10248747	0.99[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10249481	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10251015	1.00[ASN][1000 genomes]
rs10251141	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10251600	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10253091	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10256989	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10263856	0.92[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10266725	0.92[EUR][1000 genomes]
rs10268126	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10268428	0.89[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10270625	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10274013	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10279195	0.92[EUR][1000 genomes]
rs10279917	0.92[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11971269	0.97[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11974081	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11974849	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11975276	0.83[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11975863	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11976041	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11980713	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11981268	0.97[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11981966	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17140565	0.92[EUR][1000 genomes]
rs17140629	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17423728	0.92[EUR][1000 genomes]
rs2717334	1.00[ASN][1000 genomes]
rs28399914	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28572026	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28579949	0.92[EUR][1000 genomes]
rs28611415	1.00[ASN][1000 genomes]
rs28627595	0.92[EUR][1000 genomes]
rs28720702	0.92[EUR][1000 genomes]
rs28753114	0.94[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28797565	0.97[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28803198	0.94[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28820332	0.92[EUR][1000 genomes]
rs2892914	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60744788	1.00[ASN][1000 genomes]
rs60781112	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6943143	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6945718	0.92[EUR][1000 genomes]
rs6948617	1.00[ASN][1000 genomes]
rs6950144	0.92[EUR][1000 genomes]
rs6953130	1.00[ASN][1000 genomes]
rs6960648	0.92[EUR][1000 genomes]
rs6964820	0.92[EUR][1000 genomes]
rs6965235	0.92[EUR][1000 genomes]
rs6970557	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6971116	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6972974	0.92[EUR][1000 genomes];1.00[ASN][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	nsv531020	chr7:18971153-19261019	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv887817	chr7:19021592-19100076	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region lncRNA	1 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	chr7:19064400-19084800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr7:19064400-19084800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:19070400-19082200	Weak transcription	HSMM	muscle
4	chr7:19071600-19081400	Weak transcription	NHDF-Ad	bronchial
5	chr7:19075600-19089400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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