Variant report

Variant	rs2025613
Chromosome Location	chr1:78618191-78618192
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs1039865	0.80[AMR][1000 genomes]
rs11162415	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11162417	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11162418	0.95[ASN][1000 genomes]
rs11162420	0.95[ASN][1000 genomes]
rs11162421	0.95[ASN][1000 genomes]
rs11162422	0.95[ASN][1000 genomes]
rs11162423	0.93[ASN][1000 genomes]
rs11579434	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11584032	0.95[ASN][1000 genomes]
rs12082228	0.94[ASN][1000 genomes]
rs12083265	0.95[ASN][1000 genomes]
rs12131414	0.95[ASN][1000 genomes]
rs12133075	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12749252	0.95[ASN][1000 genomes]
rs12758374	0.87[CEU][hapmap]
rs1359043	0.95[ASN][1000 genomes]
rs1407747	0.81[ASN][1000 genomes]
rs1407748	0.81[ASN][1000 genomes]
rs1621088	0.95[ASN][1000 genomes]
rs1625234	0.81[ASN][1000 genomes]
rs1770306	0.94[ASN][1000 genomes]
rs1770307	0.82[JPT][hapmap];0.80[ASN][1000 genomes]
rs2025610	0.95[ASN][1000 genomes]
rs2025611	0.95[ASN][1000 genomes]
rs2025612	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2025614	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2209472	0.95[ASN][1000 genomes]
rs2351907	0.95[ASN][1000 genomes]
rs2351909	0.95[ASN][1000 genomes]
rs2351910	0.95[ASN][1000 genomes]
rs2882796	0.93[ASN][1000 genomes]
rs2882797	0.93[ASN][1000 genomes]
rs2882798	0.95[ASN][1000 genomes]
rs4258183	0.95[ASN][1000 genomes]
rs4258184	0.81[ASN][1000 genomes]
rs4268312	0.95[ASN][1000 genomes]
rs4285658	0.81[ASN][1000 genomes]
rs4396076	0.96[ASN][1000 genomes]
rs4529663	0.95[ASN][1000 genomes]
rs4587522	0.95[ASN][1000 genomes]
rs4650313	0.95[ASN][1000 genomes]
rs4650315	0.95[ASN][1000 genomes]
rs488469	0.85[ASN][1000 genomes]
rs501774	0.85[ASN][1000 genomes]
rs513245	0.85[ASN][1000 genomes]
rs513977	0.85[ASN][1000 genomes]
rs558643	0.82[ASN][1000 genomes]
rs561289	0.85[ASN][1000 genomes]
rs577978	0.86[JPT][hapmap]
rs581926	0.92[ASN][1000 genomes]
rs582795	0.80[ASN][1000 genomes]
rs584660	0.87[JPT][hapmap]
rs585100	0.86[JPT][hapmap]
rs58611517	0.95[ASN][1000 genomes]
rs596803	0.87[ASN][1000 genomes]
rs597272	0.80[ASN][1000 genomes]
rs599386	0.81[CHB][hapmap];0.92[JPT][hapmap];0.95[ASN][1000 genomes]
rs605659	0.88[JPT][hapmap]
rs60588097	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs610508	0.80[ASN][1000 genomes]
rs614963	0.87[JPT][hapmap]
rs61777350	0.92[ASN][1000 genomes]
rs618551	0.85[ASN][1000 genomes]
rs618593	0.85[ASN][1000 genomes]
rs619749	0.83[ASN][1000 genomes]
rs624766	0.85[ASN][1000 genomes]
rs627493	0.94[ASN][1000 genomes]
rs627549	0.94[ASN][1000 genomes]
rs627661	0.87[JPT][hapmap]
rs634741	0.80[ASN][1000 genomes]
rs637943	0.85[ASN][1000 genomes]
rs642248	0.86[JPT][hapmap]
rs6424716	0.95[ASN][1000 genomes]
rs6424717	0.95[ASN][1000 genomes]
rs649502	0.94[ASN][1000 genomes]
rs651413	0.89[ASN][1000 genomes]
rs656372	0.85[ASN][1000 genomes]
rs658212	0.85[ASN][1000 genomes]
rs659902	0.80[ASN][1000 genomes]
rs663254	0.86[JPT][hapmap]
rs672391	0.85[ASN][1000 genomes]
rs675799	0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs680143	0.92[ASN][1000 genomes]
rs684657	0.98[ASN][1000 genomes]
rs687708	0.88[JPT][hapmap]
rs688570	0.88[ASN][1000 genomes]
rs699009	0.85[ASN][1000 genomes]
rs72688712	0.83[ASN][1000 genomes]
rs7367729	0.94[ASN][1000 genomes]
rs7417073	0.95[ASN][1000 genomes]
rs7524877	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7532752	0.95[ASN][1000 genomes]
rs7555504	0.95[ASN][1000 genomes]
rs9425188	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013008	chr1:78463173-78958701	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv535012	chr1:78463173-78958701	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv871835	chr1:78528803-79501129	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	esv1850497	chr1:78596312-78645701	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:78584200-78630600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr1:78609200-78624600	Weak transcription	Pancreas	Pancrea
3	chr1:78609200-78624800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr1:78609400-78619000	Weak transcription	Fetal Intestine Small	intestine
5	chr1:78609600-78620800	Weak transcription	Fetal Intestine Large	intestine
6	chr1:78611600-78631400	Weak transcription	Liver	Liver
7	chr1:78613000-78619000	Weak transcription	Duodenum Mucosa	Duodenum

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