Variant report

Variant	rs10488204
Chromosome Location	chr7:12157140-12157141
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10488200	0.99[AFR][1000 genomes]
rs10488201	0.99[AFR][1000 genomes]
rs10488202	0.99[AFR][1000 genomes]
rs10488203	0.97[AFR][1000 genomes]
rs17165583	0.83[AFR][1000 genomes]
rs17165585	0.85[AFR][1000 genomes]
rs17165586	0.85[AFR][1000 genomes]
rs17165587	0.86[AFR][1000 genomes]
rs17165589	0.99[AFR][1000 genomes]
rs17165590	0.99[AFR][1000 genomes]
rs17165591	1.00[AFR][1000 genomes]
rs17165598	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17165601	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17165602	0.99[AFR][1000 genomes]
rs17165605	0.99[AFR][1000 genomes]
rs17165607	0.99[AFR][1000 genomes]
rs17165608	0.99[AFR][1000 genomes]
rs17165609	0.99[AFR][1000 genomes]
rs17165617	0.99[AFR][1000 genomes]
rs17165620	0.99[AFR][1000 genomes]
rs17165621	0.99[AFR][1000 genomes]
rs17165622	0.99[AFR][1000 genomes]
rs7777276	1.00[AFR][1000 genomes]
rs7790766	1.00[AFR][1000 genomes]
rs7791073	1.00[AFR][1000 genomes]
rs7791085	0.89[AFR][1000 genomes]
rs7807215	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv887614	chr7:11778424-12211198	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv830906	chr7:12001764-12177869	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1023608	chr7:12064114-12247520	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv534432	chr7:12148960-12693032	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12151800-12159800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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