Variant report

Variant	rs10516927
Chromosome Location	chr4:94539295-94539296
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10516939	0.87[ASN][1000 genomes]
rs1108562	0.81[ASN][1000 genomes]
rs1108563	0.92[ASN][1000 genomes]
rs12710872	0.81[ASN][1000 genomes]
rs1369467	0.81[ASN][1000 genomes]
rs1435476	0.95[ASN][1000 genomes]
rs17356606	0.95[ASN][1000 genomes]
rs17356703	0.95[ASN][1000 genomes]
rs1972861	0.87[ASN][1000 genomes]
rs58858797	1.00[ASN][1000 genomes]
rs60954238	0.87[ASN][1000 genomes]
rs6836410	0.87[ASN][1000 genomes]
rs6856877	0.92[ASN][1000 genomes]
rs6857089	0.89[ASN][1000 genomes]
rs72873020	0.87[ASN][1000 genomes]
rs72873048	0.87[ASN][1000 genomes]
rs72889182	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3584808	chr4:94156602-94559327	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1008055	chr4:94169131-95030074	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv931979	chr4:94289958-95121723	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv830009	chr4:94438751-94632656	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv821636	chr4:94439636-95116590	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	esv2830335	chr4:94440026-94629367	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1013018	chr4:94526959-94735442	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv436959	chr4:94535897-94540966	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:94538600-94539400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr4:94538800-94539400	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr4:94539000-94539600	Enhancers	Brain Angular Gyrus	brain
4	chr4:94539200-94539800	Enhancers	Brain Cingulate Gyrus	brain
5	chr4:94539200-94539800	Enhancers	Brain Substantia Nigra	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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