Variant report

Variant	rs7794124
Chromosome Location	chr7:146041727-146041728
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10243984	0.92[ASN][1000 genomes]
rs10255068	0.92[ASN][1000 genomes]
rs10255186	0.92[ASN][1000 genomes]
rs10276235	0.92[ASN][1000 genomes]
rs10277301	0.96[ASN][1000 genomes]
rs10282451	0.96[ASN][1000 genomes]
rs2693299	0.89[ASN][1000 genomes]
rs28379982	0.84[ASN][1000 genomes]
rs28512358	0.84[ASN][1000 genomes]
rs58749345	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs59186277	0.92[ASN][1000 genomes]
rs6958305	0.84[ASN][1000 genomes]
rs6973230	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6973797	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73162171	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73162193	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73162194	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73162195	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73162196	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7790714	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7795585	0.92[ASN][1000 genomes]
rs7807111	0.96[ASN][1000 genomes]
rs802506	0.92[ASN][1000 genomes]
rs802508	0.88[ASN][1000 genomes]
rs802510	0.88[ASN][1000 genomes]
rs802511	0.92[ASN][1000 genomes]
rs802512	0.92[ASN][1000 genomes]
rs802513	0.92[ASN][1000 genomes]
rs802514	0.92[ASN][1000 genomes]
rs802526	0.92[ASN][1000 genomes]
rs802527	0.92[ASN][1000 genomes]
rs802558	0.88[ASN][1000 genomes]
rs802559	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889384	chr7:145541783-146239545	Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1020950	chr7:145683419-146264304	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv889387	chr7:145903862-146239545	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv533345	chr7:145934546-146134958	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv933136	chr7:145995920-146076835	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv889388	chr7:145998111-146082957	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv524528	chr7:145998111-146086322	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv889389	chr7:145998111-146121539	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv934010	chr7:146006146-146076835	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv933530	chr7:146016273-146076835	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv608929	chr7:146020936-146082957	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv608930	chr7:146025509-146081452	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv971189	chr7:146037836-146042438	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146041400-146042400	Weak transcription	Fetal Brain Female	brain
2	chr7:146041600-146042000	Enhancers	Ovary	ovary
3	chr7:146041600-146043400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr7:146041600-146043400	Enhancers	Fetal Brain Male	brain

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