Variant report

Variant	esv2762637
Chromosome Location	chr2:53783253-53871596
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	ATF3	chr2:53786595-53787107	HCT-116	colon:	n/a	n/a
3	ATF3	chr2:53786715-53787135	HCT-116	colon:	n/a	n/a
4	BACH1	chr2:53859519-53859695	K562	blood:	n/a	n/a
5	BHLHE40	chr2:53788428-53788646	HepG2	liver:	n/a	n/a
6	BHLHE40	chr2:53844416-53844753	HepG2	liver:	n/a	n/a
7	BHLHE40	chr2:53844382-53844751	K562	blood:	n/a	n/a
8	BRCA1	chr2:53789639-53789689	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr2:53786689-53787220	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr2:53786670-53787211	HCT-116	colon:	n/a	n/a
11	CEBPB	chr2:53789586-53789943	K562	blood:	n/a	chr2:53789749-53789760
12	CEBPB	chr2:53832665-53832917	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr2:53789476-53789920	HCT-116	colon:	n/a	chr2:53789749-53789760
14	CEBPB	chr2:53786702-53787114	MCF-7	breast:	n/a	chr2:53786937-53786948
15	CEBPB	chr2:53795619-53795883	MCF-7	breast:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
16	CEBPB	chr2:53789454-53789990	MCF-7	breast:	n/a	chr2:53789749-53789760
17	CEBPB	chr2:53853060-53853166	HepG2	liver:	n/a	chr2:53853090-53853101
18	CEBPB	chr2:53804310-53804615	K562	blood:	n/a	chr2:53804453-53804464
19	CEBPB	chr2:53795595-53795940	Hela-S3	cervix:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
20	CEBPB	chr2:53795612-53795942	HepG2	liver:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
21	CEBPB	chr2:53804321-53804582	IMR90	lung:	n/a	chr2:53804453-53804464
22	CEBPB	chr2:53795589-53795907	ECC-1	luminal epithelium:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
23	CEBPB	chr2:53843211-53843390	K562	blood:	n/a	chr2:53843251-53843264 chr2:53843252-53843263
24	CEBPB	chr2:53795596-53795941	A549	lung:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
25	CEBPB	chr2:53789527-53789962	Hela-S3	cervix:	n/a	chr2:53789749-53789760
26	CEBPB	chr2:53837658-53837919	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:53789661-53789917	H1-hESC	embryonic stem cell:	n/a	chr2:53789749-53789760
28	CEBPB	chr2:53786621-53787131	Hela-S3	cervix:	n/a	chr2:53786937-53786948
29	CEBPB	chr2:53869609-53869819	A549	lung:	n/a	chr2:53869741-53869750 chr2:53869751-53869762 chr2:53869739-53869750 chr2:53869753-53869764
30	CEBPB	chr2:53789569-53789929	IMR90	lung:	n/a	chr2:53789749-53789760
31	CEBPB	chr2:53804303-53804543	HepG2	liver:	n/a	chr2:53804453-53804464
32	CEBPB	chr2:53789530-53789931	MCF-7	breast:	n/a	chr2:53789749-53789760
33	CEBPB	chr2:53795638-53795866	K562	blood:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
34	CEBPB	chr2:53784458-53784658	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:53786452-53787275	HCT-116	colon:	n/a	chr2:53786937-53786948
36	CEBPB	chr2:53869575-53869911	HepG2	liver:	n/a	chr2:53869741-53869750 chr2:53869751-53869762 chr2:53869739-53869750 chr2:53869753-53869764
37	CEBPB	chr2:53786629-53787116	MCF-7	breast:	n/a	chr2:53786937-53786948
38	CEBPB	chr2:53810690-53810961	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:53824394-53824714	HepG2	liver:	n/a	chr2:53824617-53824628 chr2:53824562-53824573 chr2:53824621-53824632 chr2:53824524-53824535 chr2:53824621-53824632
40	CEBPB	chr2:53824449-53824637	Hela-S3	cervix:	n/a	chr2:53824617-53824628 chr2:53824562-53824573 chr2:53824621-53824632 chr2:53824524-53824535 chr2:53824621-53824632
41	CEBPB	chr2:53786518-53787262	HCT-116	colon:	n/a	chr2:53786937-53786948
42	CEBPB	chr2:53843103-53843305	HepG2	liver:	n/a	chr2:53843251-53843264 chr2:53843252-53843263
43	CEBPB	chr2:53795583-53795925	IMR90	lung:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
44	CEBPB	chr2:53860540-53860903	HepG2	liver:	n/a	chr2:53860716-53860727
45	CEBPB	chr2:53789566-53789937	HepG2	liver:	n/a	chr2:53789749-53789760
46	CEBPB	chr2:53859980-53860232	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:53860000-53860240	IMR90	lung:	n/a	n/a
48	CEBPB	chr2:53789571-53789923	ECC-1	luminal epithelium:	n/a	chr2:53789749-53789760
49	CEBPB	chr2:53857472-53857527	HepG2	liver:	n/a	n/a
50	CEBPB	chr2:53786757-53787084	A549	lung:	n/a	chr2:53786937-53786948

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:53803878-53803928	HL-60	blood:	n/a
2	chr2:53803878-53803928	HRPEpiC	eye:	n/a
3	chr2:53803878-53803928	MCF10A-Er-Src	breast:	n/a
4	chr2:53803878-53803928	ProgFib	skin:	n/a
5	chr2:53803878-53803928	T-47D	breast:	n/a
6	chr2:53868889-53868939	HUVEC	blood vessel:	n/a
7	chr2:53814537-53814587	GM19239	blood:	n/a
8	chr2:53803878-53803928	HAEpiC	amniotic membrane:	n/a
9	chr2:53814537-53814587	HL-60	blood:	n/a
10	chr2:53814537-53814587	HRPEpiC	eye:	n/a
11	chr2:53868889-53868939	U87	brain:	n/a
12	chr2:53803878-53803928	HCF	heart:	n/a
13	chr2:53868889-53868939	SK-N-SH_RA	brain:	n/a
14	chr2:53814537-53814587	AG10803	skin:	n/a
15	chr2:53803878-53803928	SKMC	muscle:	n/a
16	chr2:53868889-53868939	MCF-7	breast:	n/a
17	chr2:53814537-53814587	NH-A	brain:	n/a
18	chr2:53803878-53803928	NT2-D1	testis:	n/a
19	chr2:53868889-53868939	GM12891	blood:	n/a
20	chr2:53814261-53814311	AG09309	skin:	n/a
21	chr2:53814537-53814587	ProgFib	skin:	n/a
22	chr2:53814261-53814311	HCT-116	colon:	n/a
23	chr2:53814537-53814587	HCPEpiC	choroid plexus:	n/a
24	chr2:53814261-53814311	CMK	blood:	n/a
25	chr2:53868889-53868939	HAEpiC	amniotic membrane:	n/a
26	chr2:53814261-53814311	Jurkat	blood:	n/a
27	chr2:53803878-53803928	AG04449	skin:	fetal
28	chr2:53814537-53814587	CMK	blood:	n/a
29	chr2:53868889-53868939	NH-A	brain:	n/a
30	chr2:53803878-53803928	HCPEpiC	choroid plexus:	n/a
31	chr2:53803878-53803928	PANC-1	pancreas:	n/a
32	chr2:53814537-53814587	HCF	heart:	n/a
33	chr2:53868889-53868939	BE2_C	brain:	n/a
34	chr2:53814537-53814587	SK-N-SH	brain:	n/a
35	chr2:53868889-53868939	RPTEC	kidney:	n/a
36	chr2:53814261-53814311	HRCEpiC	kidney:	n/a
37	chr2:53803878-53803928	AG09309	skin:	n/a
38	chr2:53814537-53814587	RPTEC	kidney:	n/a
39	chr2:53803878-53803928	RPTEC	kidney:	n/a
40	chr2:53814537-53814587	BJ	skin:	n/a
41	chr2:53814537-53814587	SK-N-MC	brain:	n/a
42	chr2:53803878-53803928	K562	blood:	n/a
43	chr2:53814261-53814311	HL-60	blood:	n/a
44	chr2:53803878-53803928	HMEC	breast:	n/a
45	chr2:53868889-53868939	HPAEpiC	pulmonary alveolar:	n/a
46	chr2:53868889-53868939	LNCaP	prostate:	n/a
47	chr2:53814261-53814311	ovcar-3	ovarian:	n/a
48	chr2:53803878-53803928	SK-N-MC	brain:	n/a
49	chr2:53814261-53814311	NH-A	brain:	n/a
50	chr2:53868889-53868939	Hela-S3	cervix:	n/a

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

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

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

Extended variants
information (count: 3271 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3271 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571425008	chr2:53784603-53784604	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs534746754	chr2:53784630-53784631	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs191281979	chr2:53784646-53784647	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs116211145	chr2:53784651-53784652	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs72791563	chr2:53784653-53784654	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs183142537	chr2:53784672-53784673	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs186001507	chr2:53784731-53784732	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs569638476	chr2:53784748-53784749	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs537003963	chr2:53784774-53784775	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs558845001	chr2:53784775-53784776	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs79829600	chr2:53784793-53784794	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs78902784	chr2:53784796-53784797	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs554823753	chr2:53784824-53784825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs13005429	chr2:53784834-53784835	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs4672504	chr2:53784852-53784853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73934724	chr2:53784924-53784925	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs577222476	chr2:53784944-53784945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369313387	chr2:53784978-53784979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546287360	chr2:53785002-53785003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551210480	chr2:53785011-53785012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565037310	chr2:53785028-53785029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6746107	chr2:53785037-53785038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs190967050	chr2:53785044-53785045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34033644	chr2:53785091-53785092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561148418	chr2:53785103-53785104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6720313	chr2:53785105-53785106	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs375890227	chr2:53785107-53785108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs367835619	chr2:53785108-53785109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371620455	chr2:53785109-53785110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs397871448	chr2:53785111-53785112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376049050	chr2:53785152-53785153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs57268501	chr2:53785163-53785164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs116534779	chr2:53785190-53785191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs117312199	chr2:53785225-53785226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538322961	chr2:53785226-53785227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552272313	chr2:53785235-53785236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565467207	chr2:53785252-53785253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140659076	chr2:53785269-53785270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143789350	chr2:53785285-53785286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574791237	chr2:53785290-53785291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537754022	chr2:53785302-53785303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557035204	chr2:53785337-53785338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550415774	chr2:53785385-53785386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187573656	chr2:53785470-53785471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559860418	chr2:53785497-53785498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs151156861	chr2:53785498-53785499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541217104	chr2:53785500-53785501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561113498	chr2:53785507-53785508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140205329	chr2:53785532-53785533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550066440	chr2:53785567-53785568	Weak transcription	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:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53784600-53784800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr2:53784800-53786400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr2:53786400-53787000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr2:53786400-53787400	Enhancers	Hela-S3	cervix
5	chr2:53786400-53787600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr2:53786600-53787000	Enhancers	HMEC	breast
7	chr2:53786600-53787600	Enhancers	NHEK	skin
8	chr2:53787400-53789200	Weak transcription	Hela-S3	cervix
9	chr2:53788200-53788800	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr2:53789200-53789600	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr2:53789200-53789800	Enhancers	Hela-S3	cervix
12	chr2:53789200-53790000	Enhancers	Brain Hippocampus Middle	brain
13	chr2:53789200-53790000	Enhancers	Brain Substantia Nigra	brain
14	chr2:53789400-53789800	Enhancers	Brain Cingulate Gyrus	brain
15	chr2:53789400-53790000	Enhancers	Placenta	Placenta
16	chr2:53790400-53791000	Enhancers	Colon Smooth Muscle	Colon
17	chr2:53790600-53791200	Enhancers	Rectal Smooth Muscle	rectum
18	chr2:53791000-53792400	Weak transcription	Colon Smooth Muscle	Colon
19	chr2:53792400-53792600	Enhancers	Colon Smooth Muscle	Colon
20	chr2:53794000-53794600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr2:53794200-53795000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr2:53795000-53808800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr2:53795200-53796200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr2:53795600-53795800	Active TSS	Dnd41	blood
25	chr2:53795600-53796000	Active TSS	Brain Substantia Nigra	brain
26	chr2:53795600-53796200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:53795600-53796200	Active TSS	Aorta	Aorta
28	chr2:53795600-53796200	Enhancers	Brain Anterior Caudate	brain
29	chr2:53795600-53796200	Active TSS	A549	lung
30	chr2:53795600-53796200	Active TSS	Osteobl	bone
31	chr2:53795600-53797400	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr2:53795800-53796000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr2:53795800-53796000	Enhancers	Fetal Muscle Leg	muscle
34	chr2:53795800-53796000	Flanking Active TSS	Dnd41	blood
35	chr2:53795800-53796200	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr2:53795800-53796400	Enhancers	Brain Hippocampus Middle	brain
37	chr2:53796000-53796200	Enhancers	Brain Substantia Nigra	brain
38	chr2:53796200-53799000	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr2:53796200-53799000	Weak transcription	Brain Substantia Nigra	brain
40	chr2:53796200-53802800	Weak transcription	Brain Anterior Caudate	brain
41	chr2:53796400-53799200	Weak transcription	Brain Hippocampus Middle	brain
42	chr2:53797200-53798200	Enhancers	Pancreas	Pancrea
43	chr2:53797400-53797800	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr2:53799000-53799400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr2:53799000-53799800	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr2:53799000-53800400	Enhancers	Brain Substantia Nigra	brain
47	chr2:53799200-53800000	Enhancers	Brain Cingulate Gyrus	brain
48	chr2:53799200-53800200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:53799200-53800200	Enhancers	Brain Hippocampus Middle	brain
50	chr2:53799400-53802600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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