Variant report

Variant	rs1818704
Chromosome Location	chr15:54892404-54892405
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10220855	0.88[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11632253	0.88[CEU][hapmap];0.93[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11632366	0.85[CEU][hapmap]
rs12592900	0.84[CEU][hapmap]
rs12592914	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12708436	0.92[CEU][hapmap];0.92[YRI][hapmap];0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1850994	0.92[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1851000	0.88[CEU][hapmap];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1851005	0.87[CEU][hapmap]
rs1851010	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1972137	0.92[CEU][hapmap];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2414327	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2460605	0.85[CEU][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2460606	0.88[CEU][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2553216	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2553217	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2553220	0.88[CEU][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2553221	0.83[CEU][hapmap];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2553225	0.87[CEU][hapmap];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2681958	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2681959	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2681964	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2681965	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2681966	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2911846	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2911847	0.88[CEU][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2947001	0.88[CEU][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2947003	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs35710610	0.85[ASN][1000 genomes]
rs3848141	0.84[CEU][hapmap]
rs7174529	0.87[EUR][1000 genomes]
rs72740053	0.83[EUR][1000 genomes]
rs9284299	0.88[CEU][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817539	chr15:54132584-55095235	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1038660	chr15:54756184-55039913	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv904236	chr15:54820897-54912439	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1039548	chr15:54856965-54914519	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv569508	chr15:54876212-54904782	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv526413	chr15:54876423-54904782	Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv904237	chr15:54888537-54927484	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
8	nsv569509	chr15:54888537-54932716	Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
9	esv3312449	chr15:54890485-54893511	Strong transcription Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3312450	chr15:54890485-54893511	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases
11	esv11366	chr15:54890805-54893062	Strong transcription Weak transcription	n/a	n/a	inside rSNPs	diseases
12	nsv569510	chr15:54891480-54892583	Strong transcription	n/a	n/a	inside rSNPs	diseases
13	nsv569511	chr15:54891480-54892747	Strong transcription	n/a	n/a	inside rSNPs	diseases
14	nsv569512	chr15:54891480-54893011	Strong transcription Weak transcription	n/a	n/a	inside rSNPs	diseases
15	nsv569513	chr15:54891531-54893011	Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases
16	nsv569514	chr15:54891587-54893011	Strong transcription Weak transcription	n/a	n/a	inside rSNPs	diseases
17	nsv569515	chr15:54891816-54892747	Strong transcription	n/a	n/a	inside rSNPs	diseases
18	nsv569516	chr15:54891816-54893011	Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54887600-54892800	Strong transcription	Fetal Heart	heart

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