Variant report

Variant	rs10875132
Chromosome Location	chr1:98647271-98647272
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1032196	0.82[ASN][1000 genomes]
rs10493900	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10518654	0.85[ASN][1000 genomes]
rs10783085	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10875130	0.88[ASN][1000 genomes]
rs10875131	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11165951	0.82[ASN][1000 genomes]
rs11165952	0.82[ASN][1000 genomes]
rs11165954	0.82[ASN][1000 genomes]
rs11165955	0.82[ASN][1000 genomes]
rs11165956	0.82[ASN][1000 genomes]
rs11165957	0.82[ASN][1000 genomes]
rs11165958	0.82[ASN][1000 genomes]
rs11165961	0.82[ASN][1000 genomes]
rs11165964	0.86[ASN][1000 genomes]
rs11580992	0.85[ASN][1000 genomes]
rs11802316	0.85[ASN][1000 genomes]
rs11807935	0.82[ASN][1000 genomes]
rs11809431	0.82[ASN][1000 genomes]
rs11809984	0.86[ASN][1000 genomes]
rs12021635	0.82[ASN][1000 genomes]
rs12021663	0.82[ASN][1000 genomes]
rs12027634	0.85[ASN][1000 genomes]
rs12033249	0.88[ASN][1000 genomes]
rs12038627	0.85[ASN][1000 genomes]
rs12043365	0.82[ASN][1000 genomes]
rs12044342	0.82[ASN][1000 genomes]
rs12046836	0.82[ASN][1000 genomes]
rs12401542	0.82[ASN][1000 genomes]
rs12407126	0.85[ASN][1000 genomes]
rs12407367	0.85[ASN][1000 genomes]
rs12567176	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12567725	0.82[ASN][1000 genomes]
rs12734525	0.89[ASN][1000 genomes]
rs1352254	0.82[ASN][1000 genomes]
rs1487289	0.82[ASN][1000 genomes]
rs1487302	0.82[ASN][1000 genomes]
rs17117613	0.85[ASN][1000 genomes]
rs17117616	0.85[ASN][1000 genomes]
rs17117677	0.85[ASN][1000 genomes]
rs17117759	0.82[ASN][1000 genomes]
rs17117764	0.82[ASN][1000 genomes]
rs17117766	0.82[ASN][1000 genomes]
rs17117881	0.97[ASN][1000 genomes]
rs1911501	0.85[ASN][1000 genomes]
rs1911502	0.85[ASN][1000 genomes]
rs2046585	0.82[ASN][1000 genomes]
rs2055686	0.85[ASN][1000 genomes]
rs2200583	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs355373	0.85[ASN][1000 genomes]
rs355376	0.85[ASN][1000 genomes]
rs355377	0.85[ASN][1000 genomes]
rs355379	0.85[ASN][1000 genomes]
rs4950093	0.85[ASN][1000 genomes]
rs4950094	0.85[ASN][1000 genomes]
rs4950095	0.85[ASN][1000 genomes]
rs4950096	0.82[ASN][1000 genomes]
rs4950097	0.86[ASN][1000 genomes]
rs6664310	0.85[ASN][1000 genomes]
rs7525127	0.85[ASN][1000 genomes]
rs7533634	0.85[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	nsv1012958	chr1:98081528-98864746	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv830736	chr1:98488491-98663726	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
3	nsv823631	chr1:98554257-98687985	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1010393	chr1:98643684-98698557	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:98646400-98647400	Enhancers	Hela-S3	cervix
2	chr1:98646400-98648400	Enhancers	Fetal Intestine Large	intestine
3	chr1:98646400-98648400	Enhancers	Fetal Intestine Small	intestine
4	chr1:98647200-98647600	Enhancers	Duodenum Mucosa	Duodenum
5	chr1:98647200-98647600	Enhancers	Stomach Mucosa	stomach
6	chr1:98647200-98669000	Weak transcription	HUVEC	blood vessel

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