Variant report

Variant	nsv535719
Chromosome Location	chr2:53791985-53869651
allele	n/a
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	ARID3A	chr2:53860684-53860904	HepG2	liver:	n/a	n/a
2	BACH1	chr2:53859519-53859695	K562	blood:	n/a	n/a
3	BHLHE40	chr2:53844416-53844753	HepG2	liver:	n/a	n/a
4	BHLHE40	chr2:53844382-53844751	K562	blood:	n/a	n/a
5	CEBPB	chr2:53869609-53869819	A549	lung:	n/a	chr2:53869741-53869750 chr2:53869751-53869762 chr2:53869739-53869750 chr2:53869753-53869764
6	CEBPB	chr2:53821343-53821832	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr2:53824394-53824714	HepG2	liver:	n/a	chr2:53824617-53824628 chr2:53824562-53824573 chr2:53824621-53824632 chr2:53824524-53824535 chr2:53824621-53824632
8	CEBPB	chr2:53859980-53860232	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:53795596-53795941	A549	lung:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
10	CEBPB	chr2:53795600-53796008	A549	lung:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
11	CEBPB	chr2:53795617-53795967	ECC-1	luminal epithelium:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
12	CEBPB	chr2:53843211-53843390	K562	blood:	n/a	chr2:53843251-53843264 chr2:53843252-53843263
13	CEBPB	chr2:53810690-53810961	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:53795619-53795883	MCF-7	breast:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
15	CEBPB	chr2:53860000-53860240	IMR90	lung:	n/a	n/a
16	CEBPB	chr2:53837658-53837919	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:53853060-53853166	HepG2	liver:	n/a	chr2:53853090-53853101
18	CEBPB	chr2:53832665-53832917	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:53795583-53795925	IMR90	lung:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
20	CEBPB	chr2:53824449-53824637	Hela-S3	cervix:	n/a	chr2:53824617-53824628 chr2:53824562-53824573 chr2:53824621-53824632 chr2:53824524-53824535 chr2:53824621-53824632
21	CEBPB	chr2:53860597-53860903	Hela-S3	cervix:	n/a	chr2:53860716-53860727
22	CEBPB	chr2:53869575-53869911	HepG2	liver:	n/a	chr2:53869741-53869750 chr2:53869751-53869762 chr2:53869739-53869750 chr2:53869753-53869764
23	CEBPB	chr2:53857472-53857527	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:53804321-53804582	IMR90	lung:	n/a	chr2:53804453-53804464
25	CEBPB	chr2:53843184-53843303	IMR90	lung:	n/a	chr2:53843251-53843264 chr2:53843252-53843263
26	CEBPB	chr2:53860540-53860903	HepG2	liver:	n/a	chr2:53860716-53860727
27	CEBPB	chr2:53804303-53804543	HepG2	liver:	n/a	chr2:53804453-53804464
28	CEBPB	chr2:53795595-53795940	Hela-S3	cervix:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
29	CEBPB	chr2:53795589-53795907	ECC-1	luminal epithelium:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
30	CEBPB	chr2:53843103-53843305	HepG2	liver:	n/a	chr2:53843251-53843264 chr2:53843252-53843263
31	CEBPB	chr2:53804310-53804615	K562	blood:	n/a	chr2:53804453-53804464
32	CEBPB	chr2:53795612-53795942	HepG2	liver:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
33	CEBPB	chr2:53795638-53795866	K562	blood:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
34	CTCF	chr2:53797240-53797390	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr2:53797271-53797320	GM12878	blood:	n/a	n/a
36	CTCF	chr2:53797221-53797337	NHEK	skin:	n/a	n/a
37	CTCF	chr2:53857472-53857662	K562	blood:	n/a	n/a
38	CTCF	chr2:53797220-53797370	HMEC	breast:	n/a	n/a
39	CTCF	chr2:53868600-53868750	A549	lung:	n/a	n/a
40	CTCF	chr2:53797240-53797390	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr2:53797200-53797350	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr2:53797200-53797350	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr2:53836820-53836970	SAEC	small airway:	n/a	n/a
44	CTCF	chr2:53797120-53797270	HMEC	breast:	n/a	n/a
45	CTCF	chr2:53857420-53857570	HepG2	liver:	n/a	n/a
46	CTCF	chr2:53797200-53797350	Caco-2	colon:	n/a	n/a
47	CTCF	chr2:53797196-53797364	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr2:53836890-53836974	K562	blood:	n/a	n/a
49	CTCF	chr2:53836860-53837010	HAc	cerebellar:	n/a	n/a
50	CTCF	chr2:53797238-53797344	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:53868889-53868939	NHDF-neo	bronchial:	n/a
2	chr2:53814537-53814587	BJ	skin:	n/a
3	chr2:53814261-53814311	A549	lung:	n/a
4	chr2:53814261-53814311	HL-60	blood:	n/a
5	chr2:53803878-53803928	IMR90	lung:	fetal
6	chr2:53814261-53814311	PANC-1	pancreas:	n/a
7	chr2:53814537-53814587	AG04450	lung:	fetal
8	chr2:53814261-53814311	ECC-1	luminal epithelium:	n/a
9	chr2:53814537-53814587	HRE	kidney:	n/a
10	chr2:53803878-53803928	U87	brain:	n/a
11	chr2:53803878-53803928	PrEC	prostate:	n/a
12	chr2:53814537-53814587	LNCaP	prostate:	n/a
13	chr2:53814261-53814311	HUVEC	blood vessel:	n/a
14	chr2:53868889-53868939	ovcar-3	ovarian:	n/a
15	chr2:53803878-53803928	AoSMC	blood vessel:	n/a
16	chr2:53803878-53803928	K562	blood:	n/a
17	chr2:53814261-53814311	Hela-S3	cervix:	n/a
18	chr2:53814537-53814587	NH-A	brain:	n/a
19	chr2:53814261-53814311	AG10803	skin:	n/a
20	chr2:53803878-53803928	Caco-2	colon:	n/a
21	chr2:53814261-53814311	NHDF-neo	bronchial:	n/a
22	chr2:53868889-53868939	IMR90	lung:	fetal
23	chr2:53814261-53814311	RPTEC	kidney:	n/a
24	chr2:53868889-53868939	HIPEpiC	eye:	n/a
25	chr2:53814537-53814587	GM12891	blood:	n/a
26	chr2:53814537-53814587	PFSK-1	brain:	n/a
27	chr2:53803878-53803928	HEK293	kidney:	embryo
28	chr2:53803878-53803928	HEEpiC	esophagus:	n/a
29	chr2:53803878-53803928	LNCaP	prostate:	n/a
30	chr2:53868889-53868939	HEEpiC	esophagus:	n/a
31	chr2:53803878-53803928	HIPEpiC	eye:	n/a
32	chr2:53868889-53868939	H1-hESC	embryonic stem cell:	embryo
33	chr2:53814261-53814311	U87	brain:	n/a
34	chr2:53803878-53803928	HCM	heart:	n/a
35	chr2:53868889-53868939	AG10803	skin:	n/a
36	chr2:53803878-53803928	H1-hESC	embryonic stem cell:	embryo
37	chr2:53814537-53814587	HCM	heart:	n/a
38	chr2:53814537-53814587	SK-N-MC	brain:	n/a
39	chr2:53803878-53803928	A549	lung:	n/a
40	chr2:53803878-53803928	HCPEpiC	choroid plexus:	n/a
41	chr2:53868889-53868939	HCPEpiC	choroid plexus:	n/a
42	chr2:53803878-53803928	HPAEpiC	pulmonary alveolar:	n/a
43	chr2:53803878-53803928	NT2-D1	testis:	n/a
44	chr2:53814261-53814311	K562	blood:	n/a
45	chr2:53814537-53814587	NB4	blood:	n/a
46	chr2:53868889-53868939	PrEC	prostate:	n/a
47	chr2:53814537-53814587	HRCEpiC	kidney:	n/a
48	chr2:53814537-53814587	T-47D	breast:	n/a
49	chr2:53868889-53868939	HRCEpiC	kidney:	n/a
50	chr2:53814261-53814311	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:53863876..53866246-chr2:53873113..53875135,2	K562	blood:
2	chr2:53847289..53849518-chr2:53852556..53854797,2	K562	blood:
3	chr2:53791197..53793053-chr2:53794870..53797027,2	K562	blood:
4	chr2:53795938..53798218-chr2:53812190..53814681,2	K562	blood:
5	chr2:53838050..53841676-chr2:53842441..53845129,3	K562	blood:
6	chr2:53858725..53860419-chr2:53862763..53864287,2	K562	blood:
7	chr2:53863042..53865954-chr2:54012885..54015128,2	K562	blood:
8	chr2:53838050..53841676-chr2:53842441..53845129,3	K562	blood:
9	chr2:53837091..53839319-chr2:53840310..53842800,2	K562	blood:
10	chr2:53791197..53793053-chr2:53794870..53797027,2	K562	blood:
11	chr2:53800207..53803097-chr2:53806024..53807990,2	K562	blood:
12	chr2:53807910..53809861-chr2:53812392..53815157,2	K562	blood:
13	chr2:53804711..53806458-chr2:53809800..53812091,2	MCF-7	breast:
14	chr2:53796597..53798405-chr2:53800976..53803366,2	MCF-7	breast:
15	chr2:53800207..53803097-chr2:53806024..53807990,2	K562	blood:
16	chr2:53802111..53805957-chr2:53807457..53810844,3	K562	blood:
17	chr2:53802111..53805957-chr2:53807457..53810844,3	K562	blood:
18	chr2:53858725..53860419-chr2:53862763..53864287,2	K562	blood:
19	chr2:53804711..53806458-chr2:53809800..53812091,2	MCF-7	breast:
20	chr2:53847289..53849518-chr2:53852556..53854797,2	K562	blood:
21	chr2:53807910..53809861-chr2:53812392..53815157,2	K562	blood:
22	chr2:53837091..53839319-chr2:53840310..53842800,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR75-6	chr2:53831895-53832052	NONHSAT070689
2	lnc-GPR75-6	chr2:53831784-53832052	NONHSAT070690
3	lnc-GPR75-6	chr2:53831411-53831558	NONHSAT070689
4	lnc-GPR75-5	chr2:53843602-53845521	ucscGeneNc_uc002rxj_1
5	lnc-GPR75-6	chr2:53833057-53833217	NONHSAT070690
6	lnc-GPR75-6	chr2:53833057-53833215	NONHSAT070689
7	lnc-GPR75-6	chr2:53833559-53833596	NONHSAT070690
8	lnc-GPR75-6	chr2:53808341-53808515	NONHSAT070689
9	lnc-GPR75-6	chr2:53830522-53830655	NONHSAT070689

Variant related genes	Relation type
RNU6-997P	TF binding region
GPR75-ASB3	TF binding region
RNU6-997P	CpG island
GPR75-ASB3	CpG island
ENSG00000115239	chromatin interactions
ENSG00000207456	chromatin interactions
ENSG00000068912	chromatin interactions

Extended variants
information (count: 2885 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2885 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs367560786	chr2:53792080-53792081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373693334	chr2:53792090-53792091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565897590	chr2:53792097-53792098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185306563	chr2:53792121-53792122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188442844	chr2:53792196-53792197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574567973	chr2:53792202-53792203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181257636	chr2:53792239-53792240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200784289	chr2:53792251-53792252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556823544	chr2:53792261-53792262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576769715	chr2:53792289-53792290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545550898	chr2:53792294-53792295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545395238	chr2:53792306-53792307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564050379	chr2:53792313-53792314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2193684	chr2:53792407-53792408	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs114905333	chr2:53792425-53792426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541573019	chr2:53792458-53792459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147776142	chr2:53792462-53792463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530988281	chr2:53792480-53792481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185028771	chr2:53792484-53792485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564758793	chr2:53792528-53792529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375550768	chr2:53792537-53792538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368751635	chr2:53792547-53792548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189889601	chr2:53792564-53792565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs12053563	chr2:53792592-53792593	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs75392392	chr2:53794013-53794014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs72895300	chr2:53794020-53794021	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs545032678	chr2:53794117-53794118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191585462	chr2:53794137-53794138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs527826113	chr2:53794141-53794142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546430208	chr2:53794173-53794174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567250660	chr2:53794176-53794177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75243497	chr2:53794200-53794201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74512942	chr2:53794236-53794237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569210793	chr2:53794238-53794239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138131377	chr2:53794244-53794245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149570787	chr2:53794246-53794247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571318057	chr2:53794270-53794271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144383733	chr2:53794306-53794307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184517989	chr2:53794350-53794351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188593774	chr2:53794364-53794365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10427210	chr2:53794396-53794397	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs556422576	chr2:53794407-53794408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576367879	chr2:53794419-53794420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs193277046	chr2:53794423-53794424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs34806477	chr2:53794430-53794431	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs185042579	chr2:53794431-53794432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541529737	chr2:53794442-53794443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373644287	chr2:53794456-53794457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs562322603	chr2:53794469-53794470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531666297	chr2:53794694-53794695	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53791000-53792400	Weak transcription	Colon Smooth Muscle	Colon
2	chr2:53792400-53792600	Enhancers	Colon Smooth Muscle	Colon
3	chr2:53794000-53794600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:53794200-53795000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr2:53795000-53808800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr2:53795200-53796200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr2:53795600-53795800	Active TSS	Dnd41	blood
8	chr2:53795600-53796000	Active TSS	Brain Substantia Nigra	brain
9	chr2:53795600-53796200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:53795600-53796200	Active TSS	Aorta	Aorta
11	chr2:53795600-53796200	Enhancers	Brain Anterior Caudate	brain
12	chr2:53795600-53796200	Active TSS	A549	lung
13	chr2:53795600-53796200	Active TSS	Osteobl	bone
14	chr2:53795600-53797400	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr2:53795800-53796000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr2:53795800-53796000	Enhancers	Fetal Muscle Leg	muscle
17	chr2:53795800-53796000	Flanking Active TSS	Dnd41	blood
18	chr2:53795800-53796200	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr2:53795800-53796400	Enhancers	Brain Hippocampus Middle	brain
20	chr2:53796000-53796200	Enhancers	Brain Substantia Nigra	brain
21	chr2:53796200-53799000	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr2:53796200-53799000	Weak transcription	Brain Substantia Nigra	brain
23	chr2:53796200-53802800	Weak transcription	Brain Anterior Caudate	brain
24	chr2:53796400-53799200	Weak transcription	Brain Hippocampus Middle	brain
25	chr2:53797200-53798200	Enhancers	Pancreas	Pancrea
26	chr2:53797400-53797800	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr2:53799000-53799400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr2:53799000-53799800	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr2:53799000-53800400	Enhancers	Brain Substantia Nigra	brain
30	chr2:53799200-53800000	Enhancers	Brain Cingulate Gyrus	brain
31	chr2:53799200-53800200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr2:53799200-53800200	Enhancers	Brain Hippocampus Middle	brain
33	chr2:53799400-53802600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr2:53799600-53800000	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr2:53799800-53801800	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr2:53800200-53803000	Weak transcription	Brain Hippocampus Middle	brain
37	chr2:53801800-53804400	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr2:53802200-53804400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:53802400-53804200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr2:53802600-53802800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr2:53802600-53804400	Enhancers	Brain Germinal Matrix	brain
42	chr2:53802800-53803000	Enhancers	NH-A	brain
43	chr2:53802800-53803200	Active TSS	Brain Anterior Caudate	brain
44	chr2:53802800-53803400	Enhancers	H1 Cell Line	embryonic stem cell
45	chr2:53802800-53803400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr2:53802800-53803800	Enhancers	HSMM	muscle
47	chr2:53802800-53804000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:53802800-53804200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr2:53802800-53804200	Enhancers	Fetal Stomach	stomach
50	chr2:53802800-53804200	Enhancers	Osteobl	bone

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