Variant report

Variant	nsv870674
Chromosome Location	chr1:47416441-47517123
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	chr1:47456846-47457081	HepG2	liver:	n/a	n/a
2	BACH1	chr1:47489244-47489445	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:47449788-47450018	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr1:47506533-47506550	GM12878	blood:	n/a	n/a
5	BRCA1	chr1:47489311-47489598	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr1:47498927-47499225	IMR90	lung:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
7	CEBPB	chr1:47485419-47485541	K562	blood:	n/a	chr1:47485446-47485457
8	CEBPB	chr1:47458008-47458201	HepG2	liver:	n/a	chr1:47458064-47458075
9	CEBPB	chr1:47424651-47424710	H1-hESC	embryonic stem cell:	n/a	chr1:47424681-47424692
10	CEBPB	chr1:47485351-47485535	HepG2	liver:	n/a	chr1:47485446-47485457
11	CEBPB	chr1:47478872-47479484	Hela-S3	cervix:	n/a	chr1:47478883-47478894
12	CEBPB	chr1:47462344-47463113	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:47426647-47426872	HepG2	liver:	n/a	chr1:47426704-47426715 chr1:47426706-47426717 chr1:47426706-47426715
14	CEBPB	chr1:47469301-47469803	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr1:47424621-47424813	HepG2	liver:	n/a	chr1:47424681-47424692
16	CEBPB	chr1:47457992-47458199	A549	lung:	n/a	chr1:47458064-47458075
17	CEBPB	chr1:47498924-47499142	MCF-7	breast:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
18	CEBPB	chr1:47462783-47463088	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:47498941-47499139	H1-hESC	embryonic stem cell:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
20	CEBPB	chr1:47498926-47499218	A549	lung:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
21	CEBPB	chr1:47426686-47426777	K562	blood:	n/a	chr1:47426704-47426715 chr1:47426706-47426717 chr1:47426706-47426715
22	CEBPB	chr1:47498905-47499216	HepG2	liver:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
23	CEBPB	chr1:47462780-47463046	K562	blood:	n/a	n/a
24	CEBPB	chr1:47498947-47499243	K562	blood:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
25	CEBPB	chr1:47492324-47492550	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr1:47462538-47463107	A549	lung:	n/a	n/a
27	CEBPB	chr1:47496150-47496401	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:47457975-47458107	K562	blood:	n/a	chr1:47458064-47458075
29	CHD1	chr1:47449455-47449653	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr1:47489249-47489669	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr1:47449063-47449366	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr1:47456760-47456910	BE2_C	brain:	n/a	n/a
33	CTCF	chr1:47467680-47467830	GM12872	blood:	n/a	n/a
34	CTCF	chr1:47468020-47468170	HCFaa	heart:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
35	CTCF	chr1:47456940-47457090	GM06990	blood:	n/a	n/a
36	CTCF	chr1:47468020-47468170	HEK293	kidney:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
37	CTCF	chr1:47467957-47468194	K562	blood:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
38	CTCF	chr1:47467900-47468050	HAc	cerebellar:	n/a	n/a
39	CTCF	chr1:47467980-47468130	HVMF	connective:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
40	CTCF	chr1:47467575-47467675	MCF-7	breast:	n/a	chr1:47467643-47467661 chr1:47467644-47467660
41	CTCF	chr1:47435140-47435290	HEK293	kidney:	n/a	n/a
42	CTCF	chr1:47468021-47468170	SK-N-SH_RA	brain:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
43	CTCF	chr1:47467661-47467680	LNCaP	prostate:	n/a	n/a
44	CTCF	chr1:47456803-47457062	ECC-1	luminal epithelium:	n/a	chr1:47456901-47456919 chr1:47456896-47456917 chr1:47456902-47456918
45	CTCF	chr1:47456840-47456990	HepG2	liver:	n/a	chr1:47456901-47456919 chr1:47456896-47456917 chr1:47456902-47456918
46	CTCF	chr1:47467906-47468371	A549	lung:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
47	CTCF	chr1:47456880-47457030	HRE	kidney:	n/a	chr1:47456901-47456919 chr1:47456896-47456917 chr1:47456902-47456918
48	CTCF	chr1:47434900-47435050	GM12864	blood:	n/a	n/a
49	CTCF	chr1:47434964-47435167	HepG2	liver:	n/a	chr1:47435074-47435095 chr1:47435079-47435097 chr1:47435084-47435092
50	CTCF	chr1:47468000-47468150	GM12870	blood:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:47488111-47488161	SK-N-MC	brain:	n/a
2	chr1:47493419-47493469	GM12891	blood:	n/a
3	chr1:47488256-47488306	ovcar-3	ovarian:	n/a
4	chr1:47488757-47488807	T-47D	breast:	n/a
5	chr1:47489539-47489589	Hela-S3	cervix:	n/a
6	chr1:47488757-47488807	NB4	blood:	n/a
7	chr1:47493419-47493469	MCF-7	breast:	n/a
8	chr1:47489776-47489826	HRPEpiC	eye:	n/a
9	chr1:47488256-47488306	PrEC	prostate:	n/a
10	chr1:47488757-47488807	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:47489543-47489593	NHDF-neo	bronchial:	n/a
12	chr1:47489543-47489593	Hepatocyte	liver:	n/a
13	chr1:47488757-47488807	HAEpiC	amniotic membrane:	n/a
14	chr1:47489539-47489589	Jurkat	blood:	n/a
15	chr1:47493419-47493469	SK-N-SH	brain:	n/a
16	chr1:47489539-47489589	AoSMC	blood vessel:	n/a
17	chr1:47488757-47488807	SAEC	small airway:	n/a
18	chr1:47488256-47488306	GM19239	blood:	n/a
19	chr1:47469065-47469115	U87	brain:	n/a
20	chr1:47488934-47488984	HRPEpiC	eye:	n/a
21	chr1:47489195-47489245	AG09319	gingival:	n/a
22	chr1:47488934-47488984	BJ	skin:	n/a
23	chr1:47514752-47514802	NH-A	brain:	n/a
24	chr1:47514752-47514802	K562	blood:	n/a
25	chr1:47488934-47488984	BE2_C	brain:	n/a
26	chr1:47489413-47489463	HRPEpiC	eye:	n/a
27	chr1:47469065-47469115	HCT-116	colon:	n/a
28	chr1:47488757-47488807	NHDF-neo	bronchial:	n/a
29	chr1:47489195-47489245	HCT-116	colon:	n/a
30	chr1:47489413-47489463	NHDF-neo	bronchial:	n/a
31	chr1:47486850-47486900	AG04450	lung:	fetal
32	chr1:47449205-47449255	HCF	heart:	n/a
33	chr1:47489195-47489245	A549	lung:	n/a
34	chr1:47488934-47488984	PrEC	prostate:	n/a
35	chr1:47489539-47489589	HEEpiC	esophagus:	n/a
36	chr1:47514752-47514802	NB4	blood:	n/a
37	chr1:47489543-47489593	AG09319	gingival:	n/a
38	chr1:47493419-47493469	HEEpiC	esophagus:	n/a
39	chr1:47469065-47469115	GM06990	blood:	n/a
40	chr1:47489282-47489332	HCM	heart:	n/a
41	chr1:47489413-47489463	Hepatocyte	liver:	n/a
42	chr1:47488256-47488306	A549	lung:	n/a
43	chr1:47449205-47449255	T-47D	breast:	n/a
44	chr1:47449205-47449255	HL-60	blood:	n/a
45	chr1:47488111-47488161	BE2_C	brain:	n/a
46	chr1:47488256-47488306	SK-N-SH_RA	brain:	n/a
47	chr1:47449205-47449255	HepG2	liver:	n/a
48	chr1:47488111-47488161	IMR90	lung:	fetal
49	chr1:47488934-47488984	NHBE	bronchial:	n/a
50	chr1:47486850-47486900	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:47497049..47498622-chr1:47515812..47517726,2	MCF-7	breast:
2	chr1:47500877..47503360-chr1:47503581..47505847,2	K562	blood:
3	chr1:47457191..47460016-chr1:47461610..47463680,2	K562	blood:
4	chr1:47462174..47464956-chr1:47466807..47468355,2	K562	blood:
5	chr1:47497049..47498622-chr1:47515812..47517726,2	MCF-7	breast:
6	chr1:47457191..47460016-chr1:47461610..47463680,2	K562	blood:
7	chr1:47481637..47484566-chr1:47494285..47496054,2	K562	blood:
8	chr1:47462174..47464956-chr1:47466807..47468355,2	K562	blood:
9	chr1:47489896..47492133-chr1:47492275..47494697,2	K562	blood:
10	chr1:47489896..47492133-chr1:47492275..47494697,2	K562	blood:
11	chr1:47481637..47484566-chr1:47494285..47496054,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP4X1-1	chr1:47418127-47418416	NONHSAT003043
2	lnc-CYP4A11-1	chr1:47417449-47417530	NONHSAT003042
3	lnc-CYP4A11-1	chr1:47416428-47416708	NONHSAT003042
4	lnc-CYP4A11-2	chr1:47468777-47469021	expReg_chr1_7623_-
5	lnc-CYP4X1-1	chr1:47417509-47417697	NONHSAT003043

Variant related genes	Relation type
CYP4A26P	TF binding region
CYP4X1	TF binding region
CYP4A44P	TF binding region
CYP4A27P	TF binding region
CYP4A43P	TF binding region
CYP4A26P	CpG island
CYP4X1	CpG island
CYP4A44P	CpG island
CYP4A27P	CpG island
CYP4A43P	CpG island
ENSG00000186377	chromatin interactions

Extended variants
information (count: 2928 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2928 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10789496	chr1:47416441-47416442	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576284795	chr1:47416442-47416443	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs543706305	chr1:47416463-47416464	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs187242148	chr1:47416520-47416521	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs566321845	chr1:47416524-47416525	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs66927251	chr1:47416526-47416527	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs536934259	chr1:47416561-47416562	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs529451135	chr1:47416606-47416607	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs541937423	chr1:47416644-47416645	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs149317678	chr1:47416649-47416650	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs559964496	chr1:47416677-47416678	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs527296397	chr1:47416736-47416737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551840506	chr1:47416829-47416830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563668017	chr1:47416844-47416845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570458792	chr1:47416864-47416865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144649098	chr1:47416881-47416882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs35584235	chr1:47416918-47416919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191074860	chr1:47416933-47416934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568288125	chr1:47416962-47416963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376798893	chr1:47417049-47417050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148714485	chr1:47417067-47417068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114382028	chr1:47417104-47417105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141392794	chr1:47417166-47417167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs180683752	chr1:47417196-47417197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs57627915	chr1:47417245-47417246	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs576020187	chr1:47417265-47417266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559650419	chr1:47417315-47417316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537384753	chr1:47417339-47417340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555619142	chr1:47417349-47417350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528278805	chr1:47417356-47417357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs78670432	chr1:47417375-47417376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10890429	chr1:47417393-47417394	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs543673293	chr1:47417433-47417434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76179037	chr1:47417445-47417446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555333003	chr1:47417538-47417539	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs146302382	chr1:47417553-47417554	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs115639449	chr1:47417574-47417575	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs564103194	chr1:47417577-47417578	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs531308808	chr1:47417620-47417621	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs550118274	chr1:47417649-47417650	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs561797430	chr1:47417658-47417659	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs201933555	chr1:47417664-47417665	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs370050358	chr1:47417676-47417677	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs547231782	chr1:47417704-47417705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571295824	chr1:47417710-47417711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185502405	chr1:47417760-47417761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114518543	chr1:47417798-47417799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551446805	chr1:47417839-47417840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs11211409	chr1:47417852-47417853	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs190213249	chr1:47417868-47417869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Neuroblastoma	21899760	CNVD
Uveal melanoma	20484589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Glioblastoma	20031968	CNVD
Leukemia	18688285	CNVD
Rett syndrome	21593744	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Adenocarcinoma	19001599	CNVD
Non-small cell lung cancer	19001599	CNVD
Squamous cell cancer	19001599	CNVD

Chromatin state (count:475 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47411800-47417600	Enhancers	Liver	Liver
2	chr1:47413800-47424400	Weak transcription	Adipose Nuclei	Adipose
3	chr1:47414200-47416600	Enhancers	Duodenum Mucosa	Duodenum
4	chr1:47415000-47421000	Weak transcription	Fetal Intestine Large	intestine
5	chr1:47415800-47417800	Weak transcription	Fetal Intestine Small	intestine
6	chr1:47415800-47426800	Weak transcription	Pancreas	Pancrea
7	chr1:47416400-47416600	Enhancers	Stomach Mucosa	stomach
8	chr1:47416400-47417000	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr1:47416600-47420600	Weak transcription	Stomach Mucosa	stomach
10	chr1:47417000-47418200	Weak transcription	Duodenum Mucosa	Duodenum
11	chr1:47417600-47418000	Weak transcription	Liver	Liver
12	chr1:47417800-47422000	Enhancers	Fetal Intestine Small	intestine
13	chr1:47418000-47419800	Enhancers	Liver	Liver
14	chr1:47418200-47418400	Enhancers	Duodenum Mucosa	Duodenum
15	chr1:47418400-47420600	Weak transcription	Duodenum Mucosa	Duodenum
16	chr1:47419400-47420000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:47420600-47421400	Enhancers	Duodenum Mucosa	Duodenum
18	chr1:47420600-47421600	Enhancers	Stomach Mucosa	stomach
19	chr1:47421000-47421600	Enhancers	Fetal Intestine Large	intestine
20	chr1:47421400-47426800	Weak transcription	Duodenum Mucosa	Duodenum
21	chr1:47421600-47425600	Weak transcription	Stomach Mucosa	stomach
22	chr1:47425600-47427600	Enhancers	Stomach Mucosa	stomach
23	chr1:47426200-47428400	Enhancers	Liver	Liver
24	chr1:47426800-47427000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr1:47426800-47427600	Enhancers	Duodenum Mucosa	Duodenum
26	chr1:47426800-47427800	Enhancers	Fetal Intestine Small	intestine
27	chr1:47426800-47428000	Enhancers	Pancreas	Pancrea
28	chr1:47427000-47427600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr1:47427400-47427800	Enhancers	Fetal Intestine Large	intestine
30	chr1:47430400-47433200	Weak transcription	Spleen	Spleen
31	chr1:47431200-47432000	Enhancers	Esophagus	oesophagus
32	chr1:47431600-47432000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr1:47433200-47433400	Enhancers	Spleen	Spleen
34	chr1:47434200-47434800	Enhancers	Liver	Liver
35	chr1:47434800-47435200	Flanking Active TSS	Liver	Liver
36	chr1:47435200-47435600	Enhancers	Liver	Liver
37	chr1:47438400-47448400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr1:47448000-47448800	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr1:47448400-47449200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr1:47448400-47449400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr1:47448400-47449800	Enhancers	Fetal Muscle Leg	muscle
42	chr1:47448400-47450400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr1:47448400-47450600	Enhancers	H9 Cell Line	embryonic stem cell
44	chr1:47448400-47450800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr1:47448400-47450800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr1:47448400-47451200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr1:47448600-47448800	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr1:47448600-47449200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr1:47448600-47450000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:47448600-47450400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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