Variant report

Variant	rs1105307
Chromosome Location	chr9:72046040-72046041
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs11138902	0.82[JPT][hapmap]
rs11138947	0.94[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap];0.83[EUR][1000 genomes]
rs11139245	0.83[JPT][hapmap]
rs11139246	0.83[JPT][hapmap]
rs11793760	0.94[EUR][1000 genomes]
rs12378318	0.86[JPT][hapmap]
rs13290847	0.82[JPT][hapmap]
rs13291679	0.86[JPT][hapmap]
rs13296504	0.87[JPT][hapmap]
rs13297121	0.82[JPT][hapmap]
rs1475641	0.82[JPT][hapmap]
rs1757956	0.89[ASN][1000 genomes]
rs1757960	0.86[ASN][1000 genomes]
rs1761292	0.89[ASN][1000 genomes]
rs1806631	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1831555	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1977552	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2253778	0.87[JPT][hapmap]
rs2297420	0.82[JPT][hapmap]
rs2309480	0.87[ASN][1000 genomes]
rs2777867	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2781530	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2781531	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2781542	0.88[EUR][1000 genomes]
rs2991690	0.84[ASN][1000 genomes]
rs2991692	0.89[ASN][1000 genomes]
rs2991693	0.90[ASN][1000 genomes]
rs4307408	0.83[JPT][hapmap]
rs4351475	0.83[JPT][hapmap]
rs4744893	0.87[JPT][hapmap]
rs4744897	0.89[ASN][1000 genomes]
rs7028920	0.87[JPT][hapmap]
rs7033137	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7856029	0.87[ASN][1000 genomes]
rs7869375	0.86[ASN][1000 genomes]
rs867365	0.87[JPT][hapmap]
rs867366	0.87[JPT][hapmap]
rs928563	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9775451	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817406	chr9:71675454-72179318	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv893429	chr9:71961923-72047337	ZNF genes & repeats Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1047593	chr9:71971536-72180583	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1035633	chr9:71995963-72176984	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv893431	chr9:72003036-72048098	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv2757340	chr9:72018246-72048098	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv2759694	chr9:72018246-72048098	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv893432	chr9:72028323-72056397	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1047666	chr9:72028458-72049592	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv1048650	chr9:72028458-72179847	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	esv2761289	chr9:72028470-72049604	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv1049763	chr9:72029588-72049592	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	esv2422080	chr9:72029600-72049028	Weak transcription Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv1045274	chr9:72032381-72049592	Weak transcription Strong transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv1048256	chr9:72032381-72067786	ZNF genes & repeats Strong transcription Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv1045239	chr9:72032381-72067942	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
17	nsv1041436	chr9:72032381-72069314	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
18	esv3396573	chr9:72033229-72054457	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
19	esv15039	chr9:72034725-72049025	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
20	esv2761532	chr9:72035189-72049604	Weak transcription Bivalent Enhancer Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
21	nsv442554	chr9:72035193-72049028	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
22	nsv1038185	chr9:72035199-72057304	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
23	esv3693030	chr9:72035847-72048477	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
24	nsv520760	chr9:72035847-72048477	Weak transcription ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
25	nsv818703	chr9:72035847-72048477	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
26	nsv1052872	chr9:72040184-72081554	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
27	nsv1037109	chr9:72040184-72120270	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
28	esv3483549	chr9:72042632-72047730	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72036600-72082600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr9:72037200-72046600	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr9:72037200-72048600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr9:72037200-72055600	Weak transcription	Fetal Lung	lung
5	chr9:72037200-72056200	Weak transcription	Fetal Muscle Leg	muscle
6	chr9:72037600-72046600	Weak transcription	Fetal Kidney	kidney
7	chr9:72040400-72046600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr9:72040800-72046800	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr9:72040800-72057400	Weak transcription	Fetal Heart	heart
10	chr9:72041200-72069600	Weak transcription	Gastric	stomach
11	chr9:72041600-72049400	Strong transcription	Liver	Liver
12	chr9:72041800-72046600	Weak transcription	Adipose Nuclei	Adipose
13	chr9:72042000-72070400	Weak transcription	Spleen	Spleen
14	chr9:72042400-72046600	Weak transcription	Brain Anterior Caudate	brain
15	chr9:72042600-72046200	Weak transcription	Aorta	Aorta
16	chr9:72042600-72048000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr9:72042800-72046600	Weak transcription	Stomach Smooth Muscle	stomach
18	chr9:72042800-72063800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr9:72043000-72046800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr9:72043200-72063800	Weak transcription	Brain Substantia Nigra	brain
21	chr9:72043400-72055400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr9:72043400-72055600	Weak transcription	Brain Angular Gyrus	brain
23	chr9:72043600-72046800	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr9:72044200-72084400	Weak transcription	Fetal Intestine Small	intestine
25	chr9:72044600-72046200	Weak transcription	Pancreas	Pancrea
26	chr9:72044800-72047000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr9:72044800-72048200	Strong transcription	Fetal Stomach	stomach
28	chr9:72045000-72048400	Strong transcription	Brain Hippocampus Middle	brain
29	chr9:72045000-72084400	Weak transcription	Fetal Intestine Large	intestine
30	chr9:72045200-72046800	Strong transcription	Brain Germinal Matrix	brain
31	chr9:72045200-72047200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr9:72045200-72048200	Strong transcription	Fetal Brain Female	brain
33	chr9:72045400-72046400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr9:72045400-72048000	Weak transcription	Fetal Muscle Trunk	muscle
35	chr9:72045400-72048400	Strong transcription	Ovary	ovary
36	chr9:72045400-72050600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr9:72045600-72047800	Strong transcription	Cortex derived primary cultured neurospheres	brain
38	chr9:72045800-72048600	Strong transcription	Brain Cingulate Gyrus	brain
39	chr9:72045800-72064200	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr9:72046000-72056400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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