Variant report

Variant	rs7091246
Chromosome Location	chr10:19311788-19311789
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10740828	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10763729	0.81[EUR][1000 genomes]
rs10763750	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10763751	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10763752	0.84[EUR][1000 genomes]
rs10763753	0.84[EUR][1000 genomes]
rs10763754	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10826664	0.81[EUR][1000 genomes]
rs10826665	0.81[EUR][1000 genomes]
rs10826690	0.81[EUR][1000 genomes]
rs10826691	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10826735	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10826742	0.92[EUR][1000 genomes]
rs11007659	0.81[EUR][1000 genomes]
rs11007830	0.85[EUR][1000 genomes]
rs1329228	0.81[EUR][1000 genomes]
rs1329229	0.80[EUR][1000 genomes]
rs1339046	0.87[EUR][1000 genomes]
rs1339053	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1339055	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1361294	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1416454	0.82[AFR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1416455	0.87[EUR][1000 genomes]
rs1416462	0.88[EUR][1000 genomes]
rs1416463	0.88[EUR][1000 genomes]
rs1538461	0.88[EUR][1000 genomes]
rs1538462	0.88[EUR][1000 genomes]
rs1538463	0.88[EUR][1000 genomes]
rs1538464	0.88[EUR][1000 genomes]
rs1887923	0.81[EUR][1000 genomes]
rs1934052	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2185201	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2686653	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2789307	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2813777	0.80[AFR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2813786	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4255444	0.88[EUR][1000 genomes]
rs4311959	0.85[EUR][1000 genomes]
rs4326693	0.88[EUR][1000 genomes]
rs4522068	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4619042	0.88[EUR][1000 genomes]
rs4633353	0.88[EUR][1000 genomes]
rs56058325	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6481617	0.81[EUR][1000 genomes]
rs7070237	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7079204	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7079419	0.81[EUR][1000 genomes]
rs7079871	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7083085	0.80[EUR][1000 genomes]
rs7085754	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7090989	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7095232	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7097875	0.88[EUR][1000 genomes]
rs7100348	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7906865	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7907800	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7907812	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7910929	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7911092	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7913804	0.80[EUR][1000 genomes]
rs7917242	0.80[EUR][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	nsv894916	chr10:19095467-19429415	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv466763	chr10:19205103-19334637	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv470925	chr10:19205103-19334637	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv947593	chr10:19205323-19340510	Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv3493336	chr10:19216608-19378036	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv3493337	chr10:19216667-19377987	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv427857	chr10:19253828-19599493	Enhancers Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv894917	chr10:19259024-19463367	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv550126	chr10:19270068-19572729	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	esv2761576	chr10:19290710-19323357	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
11	nsv1040087	chr10:19290710-19323913	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	nsv528472	chr10:19296750-19385248	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv1039061	chr10:19301914-19334758	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:19311400-19312000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr10:19311600-19312000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr10:19311600-19312000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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