Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10807824	0.81[EUR][1000 genomes]
rs11764103	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11972231	0.81[EUR][1000 genomes]
rs11981869	0.81[EUR][1000 genomes]
rs12672062	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12700616	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12700617	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12700618	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12700619	0.81[AMR][1000 genomes]
rs12700620	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12700621	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12700623	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12700624	0.81[EUR][1000 genomes]
rs12700625	0.81[EUR][1000 genomes]
rs1988282	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1988283	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6461862	0.81[EUR][1000 genomes]
rs6461864	0.81[EUR][1000 genomes]
rs6964890	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7811651	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv606424	chr7:24982529-25466521	Genic enhancers Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
2	nsv606426	chr7:25254125-25621579	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv887846	chr7:25371700-25407621	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:25389400-25390200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:25389400-25391200	Weak transcription	Duodenum Mucosa	Duodenum
3	chr7:25389400-25391200	Weak transcription	Small Intestine	intestine
4	chr7:25389600-25391200	Weak transcription	Fetal Intestine Large	intestine
5	chr7:25389600-25391200	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr7:25390000-25393600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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