Variant report

Variant	nsv871717
Chromosome Location	chr1:47449486-47524264
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	chr1:47462538-47463107	A549	lung:	n/a	n/a
7	CEBPB	chr1:47485351-47485535	HepG2	liver:	n/a	chr1:47485446-47485457
8	CEBPB	chr1:47485419-47485541	K562	blood:	n/a	chr1:47485446-47485457
9	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
10	CEBPB	chr1:47498927-47499225	IMR90	lung:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
11	CEBPB	chr1:47498926-47499218	A549	lung:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
12	CEBPB	chr1:47469301-47469803	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr1:47462344-47463113	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:47478872-47479484	Hela-S3	cervix:	n/a	chr1:47478883-47478894
15	CEBPB	chr1:47498947-47499243	K562	blood:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
16	CEBPB	chr1:47498924-47499142	MCF-7	breast:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
17	CEBPB	chr1:47496150-47496401	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:47492324-47492550	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:47462783-47463088	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:47498905-47499216	HepG2	liver:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
21	CEBPB	chr1:47457992-47458199	A549	lung:	n/a	chr1:47458064-47458075
22	CEBPB	chr1:47462780-47463046	K562	blood:	n/a	n/a
23	CEBPB	chr1:47457975-47458107	K562	blood:	n/a	chr1:47458064-47458075
24	CEBPB	chr1:47458008-47458201	HepG2	liver:	n/a	chr1:47458064-47458075
25	CHD1	chr1:47449455-47449653	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr1:47489249-47489669	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr1:47468040-47468190	GM12871	blood:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
28	CTCF	chr1:47456820-47456970	HMEC	breast:	n/a	chr1:47456901-47456919 chr1:47456896-47456917 chr1:47456902-47456918
29	CTCF	chr1:47467960-47468110	GM06990	blood:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
30	CTCF	chr1:47467899-47468245	K562	blood:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
31	CTCF	chr1:47467957-47468194	K562	blood:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
32	CTCF	chr1:47468000-47468150	GM12868	blood:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
33	CTCF	chr1:47457340-47457490	K562	blood:	n/a	n/a
34	CTCF	chr1:47468021-47468170	SK-N-SH_RA	brain:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
35	CTCF	chr1:47496049-47496142	GM13976	blood:	n/a	n/a
36	CTCF	chr1:47456717-47457055	H1-hESC	embryonic stem cell:	n/a	chr1:47456901-47456919 chr1:47456896-47456917 chr1:47456902-47456918
37	CTCF	chr1:47516976-47517025	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr1:47456800-47456950	GM12878	blood:	n/a	chr1:47456901-47456919 chr1:47456896-47456917 chr1:47456902-47456918
39	CTCF	chr1:47456884-47456942	GM13976	blood:	n/a	chr1:47456901-47456919 chr1:47456896-47456917 chr1:47456902-47456918
40	CTCF	chr1:47456759-47457038	HepG2	liver:	n/a	chr1:47456901-47456919 chr1:47456896-47456917 chr1:47456902-47456918
41	CTCF	chr1:47467597-47467680	H1-hESC	embryonic stem cell:	n/a	chr1:47467643-47467661 chr1:47467644-47467660
42	CTCF	chr1:47456740-47456890	GM12864	blood:	n/a	n/a
43	CTCF	chr1:47456687-47457114	HepG2	liver:	n/a	chr1:47456901-47456919 chr1:47456896-47456917 chr1:47456902-47456918
44	CTCF	chr1:47468040-47468190	GM12864	blood:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
45	CTCF	chr1:47467980-47468130	AoAF	blood vessel:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
46	CTCF	chr1:47456860-47457010	GM12873	blood:	n/a	chr1:47456901-47456919 chr1:47456896-47456917 chr1:47456902-47456918
47	CTCF	chr1:47468020-47468170	HBMEC	blood vessel:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
48	CTCF	chr1:47468040-47468190	K562	blood:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
49	CTCF	chr1:47456860-47457010	HEEpiC	esophagus:	n/a	chr1:47456901-47456919 chr1:47456896-47456917 chr1:47456902-47456918
50	CTCF	chr1:47488920-47489070	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:47488111-47488161	PrEC	prostate:	n/a
2	chr1:47489413-47489463	HRPEpiC	eye:	n/a
3	chr1:47488111-47488161	PrEC	prostate:	n/a
4	chr1:47489413-47489463	HRPEpiC	eye:	n/a
5	chr1:47489195-47489245	RPTEC	kidney:	n/a
6	chr1:47488256-47488306	T-47D	breast:	n/a
7	chr1:47488256-47488306	ProgFib	skin:	n/a
8	chr1:47489282-47489332	PrEC	prostate:	n/a
9	chr1:47489539-47489589	HMEC	breast:	n/a
10	chr1:47489543-47489593	HAEpiC	amniotic membrane:	n/a
11	chr1:47489195-47489245	NHBE	bronchial:	n/a
12	chr1:47488256-47488306	CMK	blood:	n/a
13	chr1:47469065-47469115	HNPCEpiC	eye:	n/a
14	chr1:47488757-47488807	HRE	kidney:	n/a
15	chr1:47493419-47493469	Caco-2	colon:	n/a
16	chr1:47489282-47489332	LNCaP	prostate:	n/a
17	chr1:47489413-47489463	GM12891	blood:	n/a
18	chr1:47489195-47489245	SK-N-SH_RA	brain:	n/a
19	chr1:47489776-47489826	PANC-1	pancreas:	n/a
20	chr1:47486850-47486900	HRCEpiC	kidney:	n/a
21	chr1:47486850-47486900	AG09309	skin:	n/a
22	chr1:47488934-47488984	SK-N-MC	brain:	n/a
23	chr1:47489543-47489593	SK-N-SH	brain:	n/a
24	chr1:47488256-47488306	AG04449	skin:	fetal
25	chr1:47493419-47493469	GM12878	blood:	n/a
26	chr1:47486850-47486900	HUVEC	blood vessel:	n/a
27	chr1:47493419-47493469	GM19239	blood:	n/a
28	chr1:47488256-47488306	Hela-S3	cervix:	n/a
29	chr1:47486850-47486900	CMK	blood:	n/a
30	chr1:47488256-47488306	PANC-1	pancreas:	n/a
31	chr1:47488111-47488161	AG04450	lung:	fetal
32	chr1:47486850-47486900	GM12892	blood:	n/a
33	chr1:47514752-47514802	MCF-7	breast:	n/a
34	chr1:47489413-47489463	ECC-1	luminal epithelium:	n/a
35	chr1:47488111-47488161	GM19239	blood:	n/a
36	chr1:47469065-47469115	PANC-1	pancreas:	n/a
37	chr1:47488256-47488306	GM06990	blood:	n/a
38	chr1:47488111-47488161	GM12892	blood:	n/a
39	chr1:47489543-47489593	ProgFib	skin:	n/a
40	chr1:47488256-47488306	NH-A	brain:	n/a
41	chr1:47489776-47489826	HepG2	liver:	n/a
42	chr1:47489282-47489332	HCPEpiC	choroid plexus:	n/a
43	chr1:47488934-47488984	SK-N-SH_RA	brain:	n/a
44	chr1:47489195-47489245	T-47D	breast:	n/a
45	chr1:47489282-47489332	H1-hESC	embryonic stem cell:	embryo
46	chr1:47488111-47488161	HCM	heart:	n/a
47	chr1:47488757-47488807	NHBE	bronchial:	n/a
48	chr1:47493419-47493469	HCT-116	colon:	n/a
49	chr1:47488256-47488306	HEEpiC	esophagus:	n/a
50	chr1:47489543-47489593	GM12878	blood:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP4A11-2	chr1:47468777-47469021	expReg_chr1_7623_-

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

Extended variants
information (count: 2200 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2200 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6680773	chr1:47449486-47449487	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556143659	chr1:47449497-47449498	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs79171009	chr1:47449566-47449567	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528780076	chr1:47449658-47449659	Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs535334344	chr1:47449719-47449720	Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs146975839	chr1:47449730-47449731	Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs572239519	chr1:47449743-47449744	Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs545867018	chr1:47449746-47449747	Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs564145314	chr1:47449801-47449802	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138138084	chr1:47449804-47449805	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543792468	chr1:47449841-47449842	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs9429123	chr1:47449844-47449845	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143713596	chr1:47449850-47449851	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs61284575	chr1:47449887-47449888	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs377420255	chr1:47449895-47449896	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544085602	chr1:47449896-47449897	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116315815	chr1:47449901-47449902	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs61411220	chr1:47449905-47449906	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562700469	chr1:47449908-47449909	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114990562	chr1:47449930-47449931	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531093295	chr1:47449979-47449980	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs552254445	chr1:47449987-47449988	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537411360	chr1:47450049-47450050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113494180	chr1:47450064-47450065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563701882	chr1:47450067-47450068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs58436476	chr1:47450071-47450072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs397864261	chr1:47450072-47450073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs397863808	chr1:47450073-47450074	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570471292	chr1:47450138-47450139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181816470	chr1:47450169-47450170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549744581	chr1:47450269-47450270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187208415	chr1:47450276-47450277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7527237	chr1:47450280-47450281	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs35899660	chr1:47450298-47450299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553564657	chr1:47450313-47450314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372976551	chr1:47450342-47450343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115670864	chr1:47450353-47450354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567613505	chr1:47450358-47450359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557873962	chr1:47450359-47450360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34059350	chr1:47450364-47450365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191999403	chr1:47450377-47450378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs180849019	chr1:47450416-47450417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs536689642	chr1:47450420-47450421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562098788	chr1:47450464-47450465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185498337	chr1:47450468-47450469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375744144	chr1:47450522-47450523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190160024	chr1:47450602-47450603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182798962	chr1:47450603-47450604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs111578234	chr1:47450620-47450621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs367977001	chr1:47450622-47450623	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	22522925	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:434 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47448400-47449800	Enhancers	Fetal Muscle Leg	muscle
2	chr1:47448400-47450400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:47448400-47450600	Enhancers	H9 Cell Line	embryonic stem cell
4	chr1:47448400-47450800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:47448400-47450800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:47448400-47451200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr1:47448600-47450000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr1:47448600-47450400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:47448600-47450800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr1:47448600-47451000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr1:47448800-47449600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr1:47448800-47449600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr1:47448800-47449600	Enhancers	Brain Germinal Matrix	brain
14	chr1:47448800-47449800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr1:47448800-47450800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr1:47449200-47449600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr1:47449200-47449800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr1:47449200-47450000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr1:47449400-47449600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr1:47449400-47450600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr1:47449600-47449800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr1:47449600-47449800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr1:47449600-47450800	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr1:47449600-47450800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr1:47449600-47450800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr1:47449800-47450000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr1:47449800-47450400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr1:47450000-47450400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr1:47450000-47450800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr1:47450000-47450800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr1:47450400-47450600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr1:47450400-47451000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr1:47457000-47457400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr1:47457000-47457400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr1:47457000-47457400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr1:47457000-47457400	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr1:47457000-47457400	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr1:47457000-47457600	Enhancers	H1 Cell Line	embryonic stem cell
39	chr1:47457000-47457600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr1:47457000-47457800	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr1:47457400-47465800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr1:47463800-47464600	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr1:47464600-47464800	Enhancers	H1 Cell Line	embryonic stem cell
44	chr1:47464600-47466000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr1:47464800-47465600	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr1:47464800-47466000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr1:47465600-47466000	Enhancers	H1 Cell Line	embryonic stem cell
48	chr1:47465800-47466000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr1:47469400-47469600	Flanking Active TSS	Hela-S3	cervix
50	chr1:47469600-47469800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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