Variant report

Variant	rs56170891
Chromosome Location	chr9:16556532-16556533
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10117448	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10121959	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10511622	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10756763	0.87[AMR][1000 genomes]
rs10962488	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10962492	0.83[AMR][1000 genomes]
rs10962493	0.82[AMR][1000 genomes]
rs10962511	0.82[AMR][1000 genomes]
rs12000426	0.83[AMR][1000 genomes]
rs12002673	0.83[AMR][1000 genomes]
rs12338548	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12343239	0.83[AMR][1000 genomes]
rs12343306	0.83[AMR][1000 genomes]
rs12350853	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12352543	0.89[AMR][1000 genomes]
rs1415473	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs16934816	0.80[AFR][1000 genomes]
rs1807023	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1927616	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1927617	0.83[AMR][1000 genomes]
rs1952345	0.82[AMR][1000 genomes]
rs2065937	0.85[AMR][1000 genomes]
rs2382808	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2382809	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2382810	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28414647	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28428651	0.82[AFR][1000 genomes]
rs28483319	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28593297	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28602416	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28714603	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28733737	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2891072	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6475059	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6475060	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6475062	0.83[AMR][1000 genomes]
rs6475063	0.83[AMR][1000 genomes]
rs7021199	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7022813	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7030387	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7035791	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7858025	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7863885	0.83[AMR][1000 genomes]
rs7870380	0.83[AMR][1000 genomes]
rs7872747	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7872838	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs943744	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs943745	0.88[AMR][1000 genomes];0.91[EUR][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	nsv530933	chr9:16251206-16830845	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv530934	chr9:16281246-16779432	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1032856	chr9:16465330-16773471	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv540073	chr9:16465330-16773471	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16542600-16564000	Weak transcription	HUVEC	blood vessel
2	chr9:16543800-16567000	Weak transcription	HSMMtube	muscle
3	chr9:16544000-16559600	Weak transcription	Small Intestine	intestine
4	chr9:16546000-16559600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr9:16546000-16559800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr9:16546000-16568400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr9:16550800-16559800	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr9:16551800-16567800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr9:16552000-16559600	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr9:16552000-16567800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr9:16552200-16559000	Weak transcription	Colon Smooth Muscle	Colon
12	chr9:16552800-16557600	Weak transcription	Fetal Intestine Large	intestine
13	chr9:16552800-16557800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr9:16552800-16558400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr9:16552800-16559800	Weak transcription	Stomach Smooth Muscle	stomach
16	chr9:16552800-16566600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr9:16552800-16570200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr9:16552800-16571000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr9:16552800-16571400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr9:16553000-16557800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr9:16553000-16559600	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr9:16553000-16570200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:16553000-16575200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr9:16554000-16559600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr9:16554600-16559800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr9:16554800-16556600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr9:16554800-16561200	Weak transcription	Osteobl	bone
28	chr9:16555800-16559200	Weak transcription	Ovary	ovary
29	chr9:16556400-16557000	Weak transcription	Duodenum Mucosa	Duodenum
30	chr9:16556400-16559400	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr9:16556400-16560200	Weak transcription	Colonic Mucosa	Colon
32	chr9:16556400-16566000	Weak transcription	Fetal Stomach	stomach
33	chr9:16556400-16569200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr9:16556400-16570600	Weak transcription	NHLF	lung
35	chr9:16556400-16575600	Weak transcription	HSMM	muscle

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