Variant report

Variant	nsv526153
Chromosome Location	chr6:29104935-29184660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:150)
CpG islands
(count:1100)
Chromatin interactive
region (count:9)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:150 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr6:29110427-29110694	K562	blood:	n/a	n/a
2	CCNT2	chr6:29173754-29173954	K562	blood:	n/a	n/a
3	CEBPB	chr6:29109974-29110510	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr6:29157980-29157997	HepG2	liver:	n/a	n/a
5	CEBPB	chr6:29114947-29115751	IMR90	lung:	n/a	chr6:29115098-29115109
6	CEBPB	chr6:29173602-29173813	K562	blood:	n/a	n/a
7	CEBPB	chr6:29114975-29115701	HepG2	liver:	n/a	chr6:29115098-29115109
8	CEBPB	chr6:29105537-29105852	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr6:29105551-29105846	IMR90	lung:	n/a	n/a
10	CEBPB	chr6:29114942-29115242	A549	lung:	n/a	chr6:29115098-29115109
11	CEBPB	chr6:29115465-29115665	A549	lung:	n/a	n/a
12	CEBPB	chr6:29114877-29115699	Hela-S3	cervix:	n/a	chr6:29115098-29115109
13	CEBPB	chr6:29105506-29105875	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:29105558-29105887	MCF-7	breast:	n/a	n/a
15	CEBPB	chr6:29105530-29105876	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr6:29105510-29105876	A549	lung:	n/a	n/a
17	CEBPB	chr6:29182043-29182319	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:29114969-29115710	K562	blood:	n/a	chr6:29115098-29115109
19	CEBPB	chr6:29114085-29114404	HepG2	liver:	n/a	chr6:29114234-29114245
20	CEBPB	chr6:29105509-29105880	K562	blood:	n/a	n/a
21	CEBPB	chr6:29114019-29114422	Hela-S3	cervix:	n/a	chr6:29114234-29114245
22	CTCF	chr6:29149658-29149777	MCF-7	breast:	n/a	n/a
23	CTCF	chr6:29180440-29180621	HepG2	liver:	n/a	n/a
24	CTCF	chr6:29120590-29120655	GM10248	blood:	n/a	n/a
25	CTCF	chr6:29149663-29149665	GM19240	blood:	n/a	n/a
26	CTCF	chr6:29114000-29114150	HEK293	kidney:	n/a	n/a
27	CTCF	chr6:29180483-29180574	HepG2	liver:	n/a	n/a
28	CTCF	chr6:29133537-29133577	MCF-7	breast:	n/a	n/a
29	CTCF	chr6:29180493-29180559	K562	blood:	n/a	n/a
30	CTCF	chr6:29141649-29141716	LNCaP	prostate:	n/a	n/a
31	CTCF	chr6:29177560-29177710	NHEK	skin:	n/a	n/a
32	CTCF	chr6:29141590-29141622	GM10248	blood:	n/a	n/a
33	CTCF	chr6:29149659-29149802	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:29180476-29180547	GM12878	blood:	n/a	n/a
35	CTCF	chr6:29149666-29149763	GM19240	blood:	n/a	n/a
36	CTCF	chr6:29114006-29114153	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr6:29113980-29114130	HCT-116	colon:	n/a	n/a
38	CTCF	chr6:29175989-29176034	K562	blood:	n/a	n/a
39	CTCF	chr6:29111835-29111843	GM13977	blood:	n/a	n/a
40	CTCF	chr6:29180497-29180563	K562	blood:	n/a	n/a
41	CTCF	chr6:29161925-29162065	LNCaP	prostate:	n/a	n/a
42	CTCF	chr6:29113985-29114155	Gliobla	brain:	n/a	n/a
43	CTCF	chr6:29177420-29177570	HCT-116	colon:	n/a	n/a
44	CTCF	chr6:29133508-29133553	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:29171800-29171950	RPTEC	kidney:	n/a	n/a
46	CTCF	chr6:29127652-29127709	GM20000	blood:	n/a	n/a
47	CTCF	chr6:29152898-29152982	GM13976	blood:	n/a	n/a
48	CTCF	chr6:29149659-29149799	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:29149648-29149802	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:29149732-29149752	K562	blood:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29127982-29128032	HCM	heart:	n/a
2	chr6:29137756-29137806	AG04450	lung:	fetal
3	chr6:29127982-29128032	HCM	heart:	n/a
4	chr6:29137756-29137806	AG04450	lung:	fetal
5	chr6:29141678-29141728	Hela-S3	cervix:	n/a
6	chr6:29127982-29128032	NB4	blood:	n/a
7	chr6:29140622-29140672	GM12891	blood:	n/a
8	chr6:29127979-29128029	GM12891	blood:	n/a
9	chr6:29133961-29134011	Hepatocyte	liver:	n/a
10	chr6:29141346-29141396	HL-60	blood:	n/a
11	chr6:29140768-29140818	SKMC	muscle:	n/a
12	chr6:29140126-29140176	AG09319	gingival:	n/a
13	chr6:29127871-29127921	HEEpiC	esophagus:	n/a
14	chr6:29140622-29140672	HCM	heart:	n/a
15	chr6:29133972-29134022	HNPCEpiC	eye:	n/a
16	chr6:29133505-29133555	Jurkat	blood:	n/a
17	chr6:29134247-29134297	NB4	blood:	n/a
18	chr6:29127979-29128029	HRPEpiC	eye:	n/a
19	chr6:29125104-29125154	T-47D	breast:	n/a
20	chr6:29133961-29134011	IMR90	lung:	fetal
21	chr6:29127982-29128032	HEEpiC	esophagus:	n/a
22	chr6:29140622-29140672	ovcar-3	ovarian:	n/a
23	chr6:29127979-29128029	HL-60	blood:	n/a
24	chr6:29133085-29133135	GM06990	blood:	n/a
25	chr6:29140768-29140818	NH-A	brain:	n/a
26	chr6:29140126-29140176	Jurkat	blood:	n/a
27	chr6:29127982-29128032	NT2-D1	testis:	n/a
28	chr6:29133085-29133135	HepG2	liver:	n/a
29	chr6:29141929-29141979	PrEC	prostate:	n/a
30	chr6:29137756-29137806	ProgFib	skin:	n/a
31	chr6:29125104-29125154	PFSK-1	brain:	n/a
32	chr6:29140768-29140818	Hela-S3	cervix:	n/a
33	chr6:29137756-29137806	MCF10A-Er-Src	breast:	n/a
34	chr6:29141678-29141728	HUVEC	blood vessel:	n/a
35	chr6:29134247-29134297	AoSMC	blood vessel:	n/a
36	chr6:29137756-29137806	NHBE	bronchial:	n/a
37	chr6:29141346-29141396	PrEC	prostate:	n/a
38	chr6:29133085-29133135	HNPCEpiC	eye:	n/a
39	chr6:29141346-29141396	Hela-S3	cervix:	n/a
40	chr6:29140622-29140672	NHDF-neo	bronchial:	n/a
41	chr6:29141929-29141979	SAEC	small airway:	n/a
42	chr6:29137756-29137806	GM06990	blood:	n/a
43	chr6:29130035-29130085	PFSK-1	brain:	n/a
44	chr6:29127982-29128032	GM12891	blood:	n/a
45	chr6:29141678-29141728	HCT-116	colon:	n/a
46	chr6:29133972-29134022	MCF-7	breast:	n/a
47	chr6:29130035-29130085	SAEC	small airway:	n/a
48	chr6:29130035-29130085	GM19239	blood:	n/a
49	chr6:29140622-29140672	SAEC	small airway:	n/a
50	chr6:29140768-29140818	AG10803	skin:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29016217..29018909-chr6:29120286..29121903,2	K562	blood:
2	chr6:29153930..29155451-chr6:29159790..29161704,2	K562	blood:
3	chr6:29183742..29186184-chr6:29187800..29190258,2	K562	blood:
4	chr6:29133273..29134852-chr6:29140182..29142699,2	K562	blood:
5	chr6:29116682..29119190-chr6:29125085..29127105,2	K562	blood:
6	chr6:29059208..29061169-chr6:29175130..29176997,2	K562	blood:
7	chr6:29056826..29059190-chr6:29178889..29180975,2	K562	blood:
8	chr6:29153930..29155451-chr6:29159790..29161704,2	K562	blood:
9	chr6:29116682..29119190-chr6:29125085..29127105,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR2J2-1	chr6:29163280-29163359	XLOC_005229
2	lnc-OR2B3-3	chr6:29111581-29111736	l_3154_chr6:29104220-29111736_testes
3	lnc-OR2J2-1	chr6:29167955-29168401	XLOC_005229
4	lnc-OR2J2-2	chr6:29141081-29141412	NONHSAT108513

No data

Variant related genes	Relation type
OR2J4P	TF binding region
OR2H4P	TF binding region
OR2N1P	TF binding region
OR2J2	TF binding region
OR2J4P	CpG island
OR2H4P	CpG island
OR2N1P	CpG island
OR2J2	CpG island
ENSG00000204700	chromatin interactions

Extended variants
information (count: 654 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:654 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533183346	chr6:29106804-29106805	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs185335825	chr6:29106837-29106838	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs572088333	chr6:29107117-29107118	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs370752985	chr6:29107133-29107134	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs114685781	chr6:29107198-29107199	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs112417466	chr6:29107238-29107239	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs185042881	chr6:29107240-29107241	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs533299278	chr6:29107265-29107266	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs192428651	chr6:29107309-29107310	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs183952339	chr6:29110024-29110025	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs549707349	chr6:29110030-29110031	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs73397891	chr6:29110143-29110144	ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs528716127	chr6:29110280-29110281	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs556429278	chr6:29110291-29110292	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs551713771	chr6:29110312-29110313	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs571795021	chr6:29110411-29110412	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs3130717	chr6:29110505-29110506	ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs570164474	chr6:29110510-29110511	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs370213164	chr6:29110511-29110512	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs576350222	chr6:29110521-29110522	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs567162442	chr6:29110534-29110535	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs143080048	chr6:29110564-29110565	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs3116845	chr6:29110584-29110585	ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs115550504	chr6:29110643-29110644	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs376597994	chr6:29110644-29110645	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs188228126	chr6:29110738-29110739	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs558510288	chr6:29110739-29110740	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs7745785	chr6:29110778-29110779	ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs7763908	chr6:29110838-29110839	ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs557384684	chr6:29110861-29110862	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs376939957	chr6:29110995-29110996	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs574095736	chr6:29110998-29110999	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs115160513	chr6:29111018-29111019	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs559760394	chr6:29111024-29111025	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs528826869	chr6:29111111-29111112	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs559960756	chr6:29111147-29111148	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs545681756	chr6:29111154-29111155	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs565343272	chr6:29111240-29111241	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs193281688	chr6:29111291-29111292	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs550422570	chr6:29111311-29111312	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs566994513	chr6:29111342-29111343	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs529720425	chr6:29111404-29111405	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs546224700	chr6:29111470-29111471	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs566122652	chr6:29111500-29111501	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs538593503	chr6:29111501-29111502	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs558769560	chr6:29111521-29111522	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs111750203	chr6:29111523-29111524	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs185450786	chr6:29111543-29111544	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs530423160	chr6:29111550-29111551	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs141761062	chr6:29111580-29111581	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29110000-29112000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:29113800-29115400	Enhancers	Hela-S3	cervix
3	chr6:29114200-29114400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr6:29114400-29114800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr6:29115000-29115200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:29154400-29154600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:29168800-29170800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:29170800-29185400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:29179800-29180200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:29180200-29180600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr6:29180600-29180800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr6:29180800-29189600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr6:29183600-29186200	Enhancers	Liver	Liver
14	chr6:29183600-29186200	Enhancers	HepG2	liver
15	chr6:29184000-29184600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr6:29184400-29185000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr6:29184400-29185000	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr6:29184400-29185000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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