Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1027694	0.93[CHB][hapmap]
rs12411158	0.81[EUR][1000 genomes]
rs1402696	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1494312	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1521520	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2389717	0.93[CHB][hapmap];0.87[ASN][1000 genomes]
rs316628	0.89[CEU][hapmap]
rs4906988	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4907047	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4907049	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4907051	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs583720	0.93[ASN][1000 genomes]
rs600674	0.93[CHB][hapmap];0.87[ASN][1000 genomes]
rs600902	0.85[ASN][1000 genomes]
rs612848	0.85[ASN][1000 genomes]
rs615468	0.90[ASN][1000 genomes]
rs615726	0.81[ASN][1000 genomes]
rs632802	0.98[ASN][1000 genomes]
rs655977	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6576697	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6703471	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs674494	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830414	chr1:84636738-84824651	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv830426	chr1:84704924-84856229	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84721600-84728200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:84727000-84729200	Weak transcription	Pancreas	Pancrea
3	chr1:84727000-84731000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr1:84727000-84732000	Weak transcription	Fetal Intestine Large	intestine
5	chr1:84727000-84732000	Weak transcription	Small Intestine	intestine
6	chr1:84727000-84732200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr1:84727200-84732000	Weak transcription	Fetal Intestine Small	intestine
8	chr1:84727400-84731600	Weak transcription	Stomach Mucosa	stomach
9	chr1:84727400-84734600	Weak transcription	A549	lung
10	chr1:84727800-84730600	Weak transcription	Rectal Mucosa Donor 31	rectum

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