Variant report

Variant	rs9302062
Chromosome Location	chr13:95966772-95966773
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr13:95966589-95967162	HCT-116	colon:	n/a	n/a
2	MYC	chr13:95966735-95967015	K562	blood:	n/a	n/a
3	FOXA1	chr13:95966585-95967157	HepG2	liver:	n/a	n/a
4	TCF7L2	chr13:95966661-95967146	Hela-S3	cervix:	n/a	n/a
5	STAT3	chr13:95966660-95967071	MCF10A-Er-Src	breast:	n/a	chr13:95966983-95966991
6	TCF7L2	chr13:95966661-95967053	MCF-7	breast:	n/a	n/a
7	BRCA1	chr13:95966541-95967031	Hela-S3	cervix:	n/a	n/a
8	FOSL2	chr13:95966715-95966968	HepG2	liver:	n/a	n/a
9	SIN3AK20	chr13:95966584-95967162	MCF-7	breast:	n/a	n/a
10	MAX	chr13:95966663-95967110	MCF-7	breast:	n/a	n/a
11	EP300	chr13:95966689-95966981	K562	blood:	n/a	chr13:95966911-95966925 chr13:95966917-95966927 chr13:95966845-95966855 chr13:95966869-95966877
12	STAT3	chr13:95966628-95967051	Hela-S3	cervix:	n/a	chr13:95966983-95966991
13	FOSL1	chr13:95966645-95966959	K562	blood:	n/a	n/a
14	FOSL1	chr13:95966531-95967143	HCT-116	colon:	n/a	n/a
15	TBL1XR1	chr13:95966553-95966998	K562	blood:	n/a	n/a
16	JUND	chr13:95966541-95967149	HCT-116	colon:	n/a	n/a
17	HNF4G	chr13:95966702-95967009	HepG2	liver:	n/a	chr13:95966763-95966777 chr13:95966920-95966928
18	GATA3	chr13:95966569-95967273	MCF-7	breast:	n/a	n/a
19	HDAC2	chr13:95966651-95967076	HepG2	liver:	n/a	chr13:95966846-95966855 chr13:95966918-95966927
20	HDAC2	chr13:95966707-95967087	MCF-7	breast:	n/a	chr13:95966846-95966855 chr13:95966918-95966927
21	MYC	chr13:95966615-95967153	MCF10A-Er-Src	breast:	n/a	n/a
22	EP300	chr13:95966649-95967080	HepG2	liver:	n/a	chr13:95966911-95966925 chr13:95966917-95966927 chr13:95966845-95966855 chr13:95966869-95966877
23	CEBPB	chr13:95966667-95967172	MCF-7	breast:	n/a	n/a
24	NR2F2	chr13:95966640-95967110	MCF-7	breast:	n/a	n/a
25	MAX	chr13:95966562-95967168	HepG2	liver:	n/a	n/a
26	RCOR1	chr13:95966640-95967079	K562	blood:	n/a	n/a
27	CHD2	chr13:95966711-95967026	Hela-S3	cervix:	n/a	n/a
28	FOXA1	chr13:95966648-95967037	HepG2	liver:	n/a	n/a
29	SMC3	chr13:95966708-95967053	Hela-S3	cervix:	n/a	chr13:95966883-95966891
30	MAZ	chr13:95966716-95966916	K562	blood:	n/a	n/a
31	JUN	chr13:95966678-95967021	HepG2	liver:	n/a	n/a
32	ARID3A	chr13:95966752-95966960	K562	blood:	n/a	n/a
33	SIN3AK20	chr13:95966637-95967178	MCF-7	breast:	n/a	n/a
34	EP300	chr13:95966678-95967113	Hela-S3	cervix:	n/a	chr13:95966911-95966925 chr13:95966917-95966927 chr13:95966845-95966855 chr13:95966869-95966877
35	MAX	chr13:95966760-95966970	K562	blood:	n/a	n/a
36	MYC	chr13:95966681-95967067	Hela-S3	cervix:	n/a	n/a
37	EP300	chr13:95966705-95967036	HepG2	liver:	n/a	chr13:95966911-95966925 chr13:95966917-95966927 chr13:95966845-95966855 chr13:95966869-95966877
38	FOS	chr13:95966599-95967130	MCF10A-Er-Src	breast:	n/a	n/a
39	MAFF	chr13:95966683-95967005	HepG2	liver:	n/a	n/a
40	ELF1	chr13:95966656-95967106	MCF-7	breast:	n/a	n/a
41	MAX	chr13:95966703-95967052	K562	blood:	n/a	n/a
42	MBD4	chr13:95966661-95967049	HepG2	liver:	n/a	n/a
43	MYC	chr13:95966681-95967085	K562	blood:	n/a	n/a
44	FOXP2	chr13:95966701-95966956	PFSK-1	brain:	n/a	n/a
45	MBD4	chr13:95966628-95967069	HepG2	liver:	n/a	n/a
46	RAD21	chr13:95966704-95967040	Hela-S3	cervix:	n/a	n/a
47	RCOR1	chr13:95966686-95967064	Hela-S3	cervix:	n/a	n/a
48	MAX	chr13:95966665-95967119	Hela-S3	cervix:	n/a	n/a
49	NFIC	chr13:95966626-95966997	HepG2	liver:	n/a	chr13:95966903-95966931
50	FOS	chr13:95966674-95967036	MCF10A-Er-Src	breast:	n/a	n/a

Variant related genes	Relation type
RNY3P8	TF binding region

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1764410	0.82[ASN][1000 genomes]
rs1764418	0.80[ASN][1000 genomes]
rs35513103	0.80[ASN][1000 genomes]
rs3751333	0.80[ASN][1000 genomes]
rs58489302	0.80[ASN][1000 genomes]
rs61974978	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61974990	0.83[AMR][1000 genomes]
rs6492778	0.80[ASN][1000 genomes]
rs7981674	0.83[AMR][1000 genomes]
rs7991113	0.83[AMR][1000 genomes]
rs7991114	0.83[AMR][1000 genomes]
rs9302063	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9516559	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9524906	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9524910	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533659	chr13:95757713-96042149	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1043019	chr13:95924585-96152616	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv900926	chr13:95927386-95972496	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv900927	chr13:95927386-95975185	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv456078	chr13:95929888-95972496	Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv562770	chr13:95929888-95972496	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv900929	chr13:95930072-95972496	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv900930	chr13:95930072-95975185	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1037673	chr13:95930191-96146554	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv541882	chr13:95930191-96146554	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv900931	chr13:95930685-95972496	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv1039391	chr13:95931369-96038728	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv471169	chr13:95931992-95972496	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv517610	chr13:95931992-96035883	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
15	nsv1047208	chr13:95935757-96036053	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
16	nsv1044162	chr13:95936858-96032829	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
17	nsv1044131	chr13:95939874-96016445	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
18	nsv1040348	chr13:95939874-96032829	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
19	nsv1042622	chr13:95939874-96038728	Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
20	esv2829991	chr13:95942492-95981856	Active TSS Enhancers Genic enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
21	esv3693403	chr13:95942492-95981856	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
22	nsv456079	chr13:95942492-96027507	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
23	nsv562771	chr13:95942492-96027507	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
24	nsv1049988	chr13:95942492-96038728	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
25	nsv1036031	chr13:95943731-96030662	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
26	nsv1053262	chr13:95943731-96032829	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
27	nsv456080	chr13:95943885-96015129	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
28	nsv562772	chr13:95943885-96015129	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
29	nsv456081	chr13:95943885-96027507	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
30	nsv562773	chr13:95943885-96027507	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
31	nsv1047902	chr13:95945118-96032829	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
32	nsv562774	chr13:95951593-96027507	Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
33	nsv562775	chr13:95955076-96027507	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
34	nsv562776	chr13:95959901-96027507	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
35	nsv562777	chr13:95962120-96027507	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95954800-95968800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr13:95956800-95968800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:95957800-95967000	Weak transcription	Fetal Intestine Small	intestine
4	chr13:95964000-95968600	Weak transcription	K562	blood
5	chr13:95966200-95967400	Enhancers	Hela-S3	cervix
6	chr13:95966200-95967600	Enhancers	Liver	Liver
7	chr13:95966200-95967800	Enhancers	HepG2	liver
8	chr13:95966600-95967000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr13:95966600-95967000	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr13:95966600-95967000	Enhancers	HMEC	breast
11	chr13:95966600-95967200	Enhancers	Fetal Intestine Large	intestine
12	chr13:95966600-95967400	Enhancers	Stomach Mucosa	stomach

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