Variant report

Variant	rs1484811
Chromosome Location	chr8:50950347-50950348
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1026963	0.91[JPT][hapmap];0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs11986031	0.86[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11987017	0.86[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11994226	0.86[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11998408	0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs12546435	0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs1471770	0.89[ASN][1000 genomes]
rs1484809	0.86[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1484810	0.86[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs16914220	0.86[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs16914234	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs16914250	1.00[CHB][hapmap];1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs16914299	1.00[CHB][hapmap];0.83[AMR][1000 genomes]
rs16914318	1.00[CHB][hapmap];0.87[AMR][1000 genomes]
rs16914321	1.00[CHB][hapmap];0.87[AMR][1000 genomes]
rs16914423	0.85[CHB][hapmap];0.87[AMR][1000 genomes]
rs16914526	1.00[CHB][hapmap]
rs1906070	1.00[CHB][hapmap];1.00[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1948001	0.87[ASN][1000 genomes]
rs1948002	0.87[ASN][1000 genomes]
rs1993680	0.84[AMR][1000 genomes]
rs203953	0.90[JPT][hapmap]
rs203964	0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs318919	0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs318922	0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs4467946	0.87[ASN][1000 genomes]
rs4873402	0.90[JPT][hapmap]
rs4873403	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs4873409	1.00[CHB][hapmap]
rs55889053	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs58489421	0.87[AMR][1000 genomes]
rs59046807	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73676252	0.87[AMR][1000 genomes]
rs7816568	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7839007	0.97[ASN][1000 genomes]
rs7845651	0.91[JPT][hapmap];0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3353749	chr8:50530807-51139242	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv916392	chr8:50827638-51395140	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1022115	chr8:50864995-50981944	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv611311	chr8:50865230-50980320	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv34788	chr8:50873247-50965438	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3479183	chr8:50873277-50965062	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1033098	chr8:50873293-50965692	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv2757272	chr8:50873293-50968942	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv2759613	chr8:50873293-51137995	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	esv3479184	chr8:50873317-50965027	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3479185	chr8:50873317-50965027	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3692982	chr8:50875494-50959622	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv1023258	chr8:50877934-50964286	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv2758621	chr8:50886593-51137995	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv611312	chr8:50930075-51011122	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv890871	chr8:50936174-51040022	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv890872	chr8:50946702-51032813	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:50945400-50952200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr8:50948000-50952400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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