Variant report

Variant	nsv878565
Chromosome Location	chr4:7421498-7455318
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:130)
CpG islands
(count:1408)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:130 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:7431462-7431555	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr4:7452670-7452924	GM12878	blood:	n/a	n/a
3	BRCA1	chr4:7436571-7436572	HepG2	liver:	n/a	n/a
4	CEBPB	chr4:7446537-7446857	HepG2	liver:	n/a	n/a
5	CEBPB	chr4:7446523-7446950	MCF-7	breast:	n/a	n/a
6	CEBPB	chr4:7446555-7446878	MCF-7	breast:	n/a	n/a
7	CEBPB	chr4:7433508-7433674	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr4:7446635-7446744	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:7437550-7437908	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:7433501-7433762	MCF-7	breast:	n/a	n/a
11	CEBPB	chr4:7446628-7446633	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr4:7433460-7433830	MCF-7	breast:	n/a	n/a
13	CEBPB	chr4:7446529-7446871	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:7446572-7446820	HepG2	liver:	n/a	n/a
15	CEBPB	chr4:7437595-7437783	HepG2	liver:	n/a	n/a
16	CHD2	chr4:7441612-7441614	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr4:7436619-7436861	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr4:7448380-7448530	HUVEC	blood vessel:	n/a	chr4:7448490-7448499
19	CTCF	chr4:7432240-7432390	NHEK	skin:	n/a	n/a
20	CTCF	chr4:7448420-7448570	HEK293	kidney:	n/a	chr4:7448490-7448499
21	CTCF	chr4:7435308-7435402	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr4:7439852-7439886	MCF-7	breast:	n/a	n/a
23	CTCF	chr4:7439780-7439930	HCM	heart:	n/a	n/a
24	CTCF	chr4:7439807-7439863	K562	blood:	n/a	n/a
25	CTCF	chr4:7439843-7439902	MCF-7	breast:	n/a	n/a
26	CTCF	chr4:7432277-7432412	NHEK	skin:	n/a	n/a
27	CTCF	chr4:7433640-7433790	HMEC	breast:	n/a	n/a
28	CTCF	chr4:7439720-7439870	HCT-116	colon:	n/a	n/a
29	CTCF	chr4:7435240-7435390	AG04449	skin:	n/a	n/a
30	CTCF	chr4:7426260-7426410	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr4:7439840-7439990	BE2_C	brain:	n/a	n/a
32	CTCF	chr4:7448440-7448541	MCF-7	breast:	n/a	chr4:7448490-7448499
33	CTCF	chr4:7436683-7436741	LNCaP	prostate:	n/a	chr4:7436701-7436719
34	CTCF	chr4:7426304-7426367	K562	blood:	n/a	n/a
35	CTCF	chr4:7448380-7448530	HBMEC	blood vessel:	n/a	chr4:7448490-7448499
36	CTCF	chr4:7448469-7448510	H1-hESC	embryonic stem cell:	n/a	chr4:7448490-7448499
37	CTCF	chr4:7453060-7453210	HFF-Myc	foreskin:	n/a	n/a
38	CTCF	chr4:7448440-7448590	MCF-7	breast:	n/a	chr4:7448490-7448499
39	CTCF	chr4:7426274-7426421	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr4:7432316-7432365	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:7448380-7448530	HepG2	liver:	n/a	chr4:7448490-7448499
42	CTCF	chr4:7439740-7439890	HCT-116	colon:	n/a	n/a
43	CTCF	chr4:7439814-7439928	MCF-7	breast:	n/a	n/a
44	CTCF	chr4:7448440-7448590	SK-N-SH_RA	brain:	n/a	chr4:7448490-7448499
45	CTCF	chr4:7432260-7432410	HMEC	breast:	n/a	n/a
46	CTCF	chr4:7439800-7439950	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr4:7426660-7426810	WERI-Rb-1	eye:	n/a	chr4:7426696-7426709
48	CTCF	chr4:7435260-7435410	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr4:7432400-7432550	HRE	kidney:	n/a	n/a
50	CTCF	chr4:7439967-7439994	Lung_OC	lung:	n/a	n/a

(count:1408 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7436199-7436249	NT2-D1	testis:	n/a
2	chr4:7436701-7436751	HCT-116	colon:	n/a
3	chr4:7427313-7427363	GM06990	blood:	n/a
4	chr4:7427313-7427363	HCPEpiC	choroid plexus:	n/a
5	chr4:7436199-7436249	A549	lung:	n/a
6	chr4:7436199-7436249	NT2-D1	testis:	n/a
7	chr4:7436701-7436751	HCT-116	colon:	n/a
8	chr4:7427313-7427363	GM06990	blood:	n/a
9	chr4:7427313-7427363	HCPEpiC	choroid plexus:	n/a
10	chr4:7436199-7436249	A549	lung:	n/a
11	chr4:7427446-7427496	GM12892	blood:	n/a
12	chr4:7438657-7438707	BJ	skin:	n/a
13	chr4:7427195-7427245	H1-hESC	embryonic stem cell:	embryo
14	chr4:7438657-7438707	HL-60	blood:	n/a
15	chr4:7436874-7436924	ECC-1	luminal epithelium:	n/a
16	chr4:7427446-7427496	HRE	kidney:	n/a
17	chr4:7449747-7449797	U87	brain:	n/a
18	chr4:7435639-7435689	HRCEpiC	kidney:	n/a
19	chr4:7449747-7449797	HEEpiC	esophagus:	n/a
20	chr4:7436693-7436743	Jurkat	blood:	n/a
21	chr4:7437027-7437077	HCT-116	colon:	n/a
22	chr4:7437027-7437077	MCF10A-Er-Src	breast:	n/a
23	chr4:7436861-7436911	HNPCEpiC	eye:	n/a
24	chr4:7449747-7449797	AG04449	skin:	fetal
25	chr4:7438657-7438707	ovcar-3	ovarian:	n/a
26	chr4:7437027-7437077	Hela-S3	cervix:	n/a
27	chr4:7436239-7436289	H1-hESC	embryonic stem cell:	embryo
28	chr4:7437027-7437077	GM19239	blood:	n/a
29	chr4:7436259-7436309	HUVEC	blood vessel:	n/a
30	chr4:7427313-7427363	NT2-D1	testis:	n/a
31	chr4:7436701-7436751	PrEC	prostate:	n/a
32	chr4:7436861-7436911	NHBE	bronchial:	n/a
33	chr4:7430936-7430986	HRPEpiC	eye:	n/a
34	chr4:7436861-7436911	HAEpiC	amniotic membrane:	n/a
35	chr4:7435463-7435513	PANC-1	pancreas:	n/a
36	chr4:7436701-7436751	Hepatocyte	liver:	n/a
37	chr4:7436239-7436289	MCF10A-Er-Src	breast:	n/a
38	chr4:7436701-7436751	SAEC	small airway:	n/a
39	chr4:7427313-7427363	HAEpiC	amniotic membrane:	n/a
40	chr4:7427446-7427496	NH-A	brain:	n/a
41	chr4:7427446-7427496	PFSK-1	brain:	n/a
42	chr4:7430936-7430986	HRCEpiC	kidney:	n/a
43	chr4:7436259-7436309	AG04450	lung:	fetal
44	chr4:7436199-7436249	RPTEC	kidney:	n/a
45	chr4:7449698-7449748	PrEC	prostate:	n/a
46	chr4:7430936-7430986	GM19239	blood:	n/a
47	chr4:7427446-7427496	Hepatocyte	liver:	n/a
48	chr4:7436874-7436924	MCF-7	breast:	n/a
49	chr4:7436259-7436309	GM19239	blood:	n/a
50	chr4:7427195-7427245	MCF-7	breast:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:7421765..7423604-chr4:7439157..7441831,2	K562	blood:
2	chr4:7444681..7447159-chr4:7457852..7459823,2	MCF-7	breast:
3	chr4:7432269..7435967-chr4:7438458..7442398,4	MCF-7	breast:
4	chr4:7428532..7430154-chr4:7431457..7433548,3	K562	blood:
5	chr4:7445641..7447880-chr4:7451112..7453216,2	K562	blood:
6	chr4:7420470..7422077-chr4:7425743..7427334,2	MCF-7	breast:
7	chr4:7436453..7438238-chr4:7441242..7443096,2	MCF-7	breast:
8	chr4:7430997..7432542-chr4:7435254..7438169,2	MCF-7	breast:
9	chr4:7420470..7422077-chr4:7425743..7427334,2	MCF-7	breast:
10	chr4:7421765..7423604-chr4:7439157..7441831,2	K562	blood:
11	chr4:7452936..7455745-chr4:7457448..7459365,2	MCF-7	breast:
12	chr4:7426666..7428188-chr4:7440042..7442576,2	MCF-7	breast:
13	chr4:7412059..7414681-chr4:7420210..7422240,3	MCF-7	breast:
14	chr4:7445641..7447880-chr4:7451112..7453216,2	K562	blood:
15	chr4:7432269..7435967-chr4:7438458..7442398,4	MCF-7	breast:
16	chr4:7426666..7428188-chr4:7440042..7442576,2	MCF-7	breast:
17	chr4:7428532..7430154-chr4:7431457..7433548,3	K562	blood:
18	chr4:7368964..7371820-chr4:7419661..7422236,2	K562	blood:
19	chr4:7430206..7433720-chr4:7434978..7437884,3	K562	blood:
20	chr4:7455060..7457538-chr4:7459563..7461357,2	K562	blood:
21	chr4:7421842..7424756-chr4:7435320..7437360,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSAPL1-1	chr4:7432021-7433304	NONHSAT095056

No data

Variant related genes	Relation type
PSAPL1	TF binding region
PSAPL1	CpG island
ENSG00000178597	chromatin interactions

Extended variants
information (count: 2033 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2033 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4689741	chr4:7421498-7421499	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574705610	chr4:7421537-7421538	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs147490774	chr4:7421549-7421550	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs563588338	chr4:7421582-7421583	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs575806497	chr4:7421632-7421633	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs546411360	chr4:7421700-7421701	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs564817507	chr4:7421747-7421748	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs528773691	chr4:7421775-7421776	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs370186862	chr4:7421777-7421778	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs539744352	chr4:7421789-7421790	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs547451439	chr4:7421874-7421875	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs187180918	chr4:7421899-7421900	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs4689742	chr4:7421900-7421901	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs4689743	chr4:7421936-7421937	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs569640232	chr4:7421948-7421949	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs139862842	chr4:7421960-7421961	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs145394074	chr4:7421963-7421964	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs4689744	chr4:7421996-7421997	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs145382496	chr4:7422007-7422008	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs13114433	chr4:7422036-7422037	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs552824053	chr4:7422045-7422046	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542026972	chr4:7422052-7422053	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs34829823	chr4:7422086-7422087	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs148800194	chr4:7422094-7422095	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs557471034	chr4:7422129-7422130	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs575647594	chr4:7422158-7422159	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546448170	chr4:7422159-7422160	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs28677109	chr4:7422161-7422162	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs117519935	chr4:7422185-7422186	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs34442888	chr4:7422196-7422197	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs13138401	chr4:7422226-7422227	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs191588693	chr4:7422258-7422259	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs528111543	chr4:7422294-7422295	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs563423154	chr4:7422304-7422305	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184458535	chr4:7422311-7422312	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546233886	chr4:7422315-7422316	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs34427823	chr4:7422325-7422326	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs368696431	chr4:7422363-7422364	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs528227408	chr4:7422368-7422369	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs7681390	chr4:7422378-7422379	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs568257088	chr4:7422380-7422381	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs550843770	chr4:7422393-7422394	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs142386352	chr4:7422408-7422409	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569048892	chr4:7422409-7422410	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs188988392	chr4:7422437-7422438	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs539955264	chr4:7422440-7422441	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs7660356	chr4:7422453-7422454	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs370046719	chr4:7422459-7422460	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs112608043	chr4:7422472-7422473	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs151306496	chr4:7422511-7422512	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7414600-7422200	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr4:7418800-7429200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:7421000-7422000	Weak transcription	Stomach Smooth Muscle	stomach
4	chr4:7421000-7422200	Bivalent Enhancer	Fetal Muscle Leg	muscle
5	chr4:7421200-7421800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
6	chr4:7421200-7422800	Enhancers	Brain Substantia Nigra	brain
7	chr4:7421400-7423000	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr4:7421600-7422200	Enhancers	Colon Smooth Muscle	Colon
9	chr4:7421600-7422800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr4:7421600-7424200	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr4:7421800-7422800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
12	chr4:7421800-7425200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr4:7422000-7422600	Enhancers	Stomach Smooth Muscle	stomach
14	chr4:7422000-7422800	Enhancers	Brain Cingulate Gyrus	brain
15	chr4:7422000-7423000	Enhancers	Esophagus	oesophagus
16	chr4:7422200-7422400	Enhancers	Duodenum Smooth Muscle	Duodenum
17	chr4:7422200-7422600	Enhancers	Brain Anterior Caudate	brain
18	chr4:7422200-7422600	Enhancers	Right Ventricle	heart
19	chr4:7422200-7422800	Enhancers	Lung	lung
20	chr4:7422200-7423000	Enhancers	Fetal Muscle Leg	muscle
21	chr4:7422400-7422800	Enhancers	Brain Angular Gyrus	brain
22	chr4:7422600-7425200	Weak transcription	Brain Anterior Caudate	brain
23	chr4:7422600-7425400	Weak transcription	Brain Hippocampus Middle	brain
24	chr4:7422800-7425400	Weak transcription	Brain Substantia Nigra	brain
25	chr4:7422800-7425600	Weak transcription	Brain Angular Gyrus	brain
26	chr4:7422800-7425600	Weak transcription	Brain Cingulate Gyrus	brain
27	chr4:7423000-7425000	Weak transcription	Fetal Muscle Leg	muscle
28	chr4:7423000-7425200	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr4:7423000-7425600	Weak transcription	Esophagus	oesophagus
30	chr4:7423200-7436200	Weak transcription	Right Atrium	heart
31	chr4:7423400-7423800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:7423800-7424000	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr4:7423800-7424000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:7424000-7424600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr4:7424000-7426400	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr4:7424200-7425600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr4:7424400-7425600	Weak transcription	Spleen	Spleen
38	chr4:7424600-7425600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:7424800-7425000	Enhancers	Brain Germinal Matrix	brain
40	chr4:7425000-7425600	Weak transcription	Brain Germinal Matrix	brain
41	chr4:7425000-7430400	Enhancers	Fetal Muscle Leg	muscle
42	chr4:7425200-7426200	Enhancers	Brain Anterior Caudate	brain
43	chr4:7425200-7426200	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr4:7425200-7426200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr4:7425200-7430400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr4:7425400-7426000	Enhancers	Brain Hippocampus Middle	brain
47	chr4:7425400-7426200	Enhancers	Brain Substantia Nigra	brain
48	chr4:7425600-7425800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr4:7425600-7425800	Enhancers	Brain Germinal Matrix	brain
50	chr4:7425600-7426200	Enhancers	Brain Cingulate Gyrus	brain

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