Variant report

Variant	nsv830012
Chromosome Location	chr4:96547783-96746163
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	ATF2	chr4:96614804-96615129	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:96614717-96615069	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr4:96720077-96720233	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr4:96720028-96720203	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr4:96603085-96603089	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr4:96597434-96597706	A549	lung:	n/a	chr4:96597565-96597576
7	CEBPB	chr4:96703659-96703859	K562	blood:	n/a	chr4:96703699-96703710 chr4:96703701-96703710
8	CEBPB	chr4:96649198-96649434	HepG2	liver:	n/a	chr4:96649277-96649288 chr4:96649328-96649339
9	CEBPB	chr4:96578583-96578682	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:96693254-96693466	HepG2	liver:	n/a	chr4:96693362-96693373
11	CEBPB	chr4:96560136-96560766	Hela-S3	cervix:	n/a	chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560342 chr4:96560331-96560340 chr4:96560555-96560566 chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560340
12	CEBPB	chr4:96693229-96693518	IMR90	lung:	n/a	chr4:96693362-96693373
13	CEBPB	chr4:96636890-96637488	MCF-7	breast:	n/a	n/a
14	CEBPB	chr4:96578513-96578622	A549	lung:	n/a	n/a
15	CEBPB	chr4:96703619-96704039	IMR90	lung:	n/a	chr4:96703699-96703710 chr4:96703701-96703710 chr4:96704005-96704016
16	CEBPB	chr4:96560276-96560665	A549	lung:	n/a	chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560342 chr4:96560331-96560340 chr4:96560555-96560566 chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560340
17	CEBPB	chr4:96560311-96560737	H1-hESC	embryonic stem cell:	n/a	chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560342 chr4:96560331-96560340 chr4:96560555-96560566 chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560340
18	CEBPB	chr4:96702003-96702220	A549	lung:	n/a	n/a
19	CEBPB	chr4:96668490-96669010	MCF-7	breast:	n/a	n/a
20	CEBPB	chr4:96560210-96560732	HepG2	liver:	n/a	chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560342 chr4:96560331-96560340 chr4:96560555-96560566 chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560340
21	CEBPB	chr4:96668531-96669056	MCF-7	breast:	n/a	chr4:96669001-96669014
22	CEBPB	chr4:96597411-96597724	HepG2	liver:	n/a	chr4:96597565-96597576
23	CEBPB	chr4:96702017-96702218	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:96560285-96560783	MCF-7	breast:	n/a	chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560342 chr4:96560331-96560340 chr4:96560555-96560566 chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560340
25	CEBPB	chr4:96703580-96703990	A549	lung:	n/a	chr4:96703699-96703710 chr4:96703701-96703710
26	CEBPB	chr4:96702036-96702236	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr4:96637023-96637373	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr4:96560260-96560742	IMR90	lung:	n/a	chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560342 chr4:96560331-96560340 chr4:96560555-96560566 chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560340
29	CEBPB	chr4:96560127-96560815	ECC-1	luminal epithelium:	n/a	chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560342 chr4:96560331-96560340 chr4:96560555-96560566 chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560340
30	CEBPB	chr4:96554016-96554017	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr4:96560136-96560732	ECC-1	luminal epithelium:	n/a	chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560342 chr4:96560331-96560340 chr4:96560555-96560566 chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560340
32	CEBPB	chr4:96649188-96649501	A549	lung:	n/a	chr4:96649277-96649288 chr4:96649328-96649339
33	CEBPB	chr4:96703666-96703970	HepG2	liver:	n/a	chr4:96703699-96703710 chr4:96703701-96703710
34	CEBPB	chr4:96636962-96637451	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr4:96653308-96653672	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr4:96636884-96637398	MCF-7	breast:	n/a	n/a
37	CEBPB	chr4:96560401-96560681	K562	blood:	n/a	chr4:96560555-96560566
38	CEBPB	chr4:96597442-96597710	IMR90	lung:	n/a	chr4:96597565-96597576
39	CEBPB	chr4:96597442-96597596	H1-hESC	embryonic stem cell:	n/a	chr4:96597565-96597576
40	CEBPB	chr4:96719923-96720273	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:96560232-96560743	A549	lung:	n/a	chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560342 chr4:96560331-96560340 chr4:96560555-96560566 chr4:96560329-96560342 chr4:96560331-96560340 chr4:96560331-96560340
42	CHD1	chr4:96719677-96719682	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr4:96723453-96723459	GM12878	blood:	n/a	n/a
44	CHD2	chr4:96719273-96719276	GM12878	blood:	n/a	n/a
45	CTCF	chr4:96558298-96558457	Pancreas_OC	pancreas:	n/a	chr4:96558374-96558387
46	CTCF	chr4:96614840-96614990	GM12865	blood:	n/a	n/a
47	CTCF	chr4:96558320-96558470	HEK293	kidney:	n/a	chr4:96558374-96558387
48	CTCF	chr4:96558282-96558467	MCF-7	breast:	n/a	chr4:96558374-96558387
49	CTCF	chr4:96614572-96615185	SK-N-SH	brain:	n/a	n/a
50	CTCF	chr4:96558320-96558470	HCM	heart:	n/a	chr4:96558374-96558387

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:96549942-96549992	GM12878	blood:	n/a
2	chr4:96549942-96549992	GM12878	blood:	n/a
3	chr4:96549942-96549992	IMR90	lung:	fetal
4	chr4:96678053-96678103	NB4	blood:	n/a
5	chr4:96678053-96678103	HRPEpiC	eye:	n/a
6	chr4:96678053-96678103	AG04449	skin:	fetal
7	chr4:96549942-96549992	GM12892	blood:	n/a
8	chr4:96678053-96678103	HCM	heart:	n/a
9	chr4:96549942-96549992	NH-A	brain:	n/a
10	chr4:96678053-96678103	Jurkat	blood:	n/a
11	chr4:96678053-96678103	Caco-2	colon:	n/a
12	chr4:96549942-96549992	HEK293	kidney:	embryo
13	chr4:96549942-96549992	HNPCEpiC	eye:	n/a
14	chr4:96549942-96549992	CMK	blood:	n/a
15	chr4:96549942-96549992	HRCEpiC	kidney:	n/a
16	chr4:96678053-96678103	HIPEpiC	eye:	n/a
17	chr4:96549942-96549992	HEEpiC	esophagus:	n/a
18	chr4:96549942-96549992	AG09309	skin:	n/a
19	chr4:96678053-96678103	AG10803	skin:	n/a
20	chr4:96549942-96549992	HUVEC	blood vessel:	n/a
21	chr4:96549942-96549992	PANC-1	pancreas:	n/a
22	chr4:96549942-96549992	LNCaP	prostate:	n/a
23	chr4:96678053-96678103	HCF	heart:	n/a
24	chr4:96549942-96549992	AG10803	skin:	n/a
25	chr4:96678053-96678103	ovcar-3	ovarian:	n/a
26	chr4:96678053-96678103	NHBE	bronchial:	n/a
27	chr4:96678053-96678103	HRE	kidney:	n/a
28	chr4:96678053-96678103	ECC-1	luminal epithelium:	n/a
29	chr4:96549942-96549992	HRE	kidney:	n/a
30	chr4:96678053-96678103	NH-A	brain:	n/a
31	chr4:96549942-96549992	K562	blood:	n/a
32	chr4:96549942-96549992	AG04450	lung:	fetal
33	chr4:96678053-96678103	ProgFib	skin:	n/a
34	chr4:96678053-96678103	HEEpiC	esophagus:	n/a
35	chr4:96678053-96678103	SK-N-SH_RA	brain:	n/a
36	chr4:96549942-96549992	PFSK-1	brain:	n/a
37	chr4:96549942-96549992	HCF	heart:	n/a
38	chr4:96678053-96678103	HepG2	liver:	n/a
39	chr4:96678053-96678103	PFSK-1	brain:	n/a
40	chr4:96678053-96678103	SAEC	small airway:	n/a
41	chr4:96549942-96549992	SAEC	small airway:	n/a
42	chr4:96678053-96678103	HCPEpiC	choroid plexus:	n/a
43	chr4:96549942-96549992	AoSMC	blood vessel:	n/a
44	chr4:96678053-96678103	HNPCEpiC	eye:	n/a
45	chr4:96678053-96678103	HEK293	kidney:	embryo
46	chr4:96549942-96549992	NHBE	bronchial:	n/a
47	chr4:96678053-96678103	U87	brain:	n/a
48	chr4:96678053-96678103	AG04450	lung:	fetal
49	chr4:96549942-96549992	A549	lung:	n/a
50	chr4:96678053-96678103	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:96674646..96677370-chr4:96678560..96681527,2	MCF-7	breast:
2	chr4:96669276..96670825-chr4:96677264..96679662,2	MCF-7	breast:
3	chr1:149223221..149225022-chr4:96577789..96580768,2	MCF-7	breast:
4	chr4:96614781..96615424-chr4:97273090..97273698,2	MCF-7	breast:
5	chr4:96669276..96670825-chr4:96677264..96679662,2	MCF-7	breast:
6	chr4:96720160..96722789-chr4:96726350..96727999,2	K562	blood:
7	chr4:96557966..96558741-chr4:97273098..97274003,3	MCF-7	breast:
8	chr4:96674646..96677370-chr4:96678560..96681527,2	MCF-7	breast:
9	chr4:96720160..96722789-chr4:96726350..96727999,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC5C-2	chr4:96566103-96566444	NONHSAT097463

Variant related genes	Relation type
RPL30P6	TF binding region
RPL30P6	CpG island
ENSG00000206737	chromatin interactions

Extended variants
information (count: 4696 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4696 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551018606	chr4:96547798-96547799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs1436570	chr4:96547808-96547809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs191419062	chr4:96547832-96547833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs9991132	chr4:96547854-96547855	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs1436571	chr4:96547918-96547919	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs535577616	chr4:96548008-96548009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs10001771	chr4:96548022-96548023	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs575120910	chr4:96548067-96548068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542835815	chr4:96548079-96548080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538038224	chr4:96548097-96548098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369337508	chr4:96548135-96548136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182741255	chr4:96548136-96548137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115646624	chr4:96548141-96548142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114140285	chr4:96548162-96548163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs35403357	chr4:96548213-96548214	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs573644134	chr4:96548216-96548217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187817306	chr4:96548260-96548261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6815247	chr4:96548278-96548279	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs531059226	chr4:96548332-96548333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551146463	chr4:96548352-96548353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73841163	chr4:96548356-96548357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377702634	chr4:96548357-96548358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564484064	chr4:96548358-96548359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532631980	chr4:96548433-96548434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191149217	chr4:96548539-96548540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183472534	chr4:96548547-96548548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6820560	chr4:96548558-96548559	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs187759455	chr4:96548574-96548575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568998405	chr4:96548586-96548587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537908129	chr4:96548587-96548588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373067391	chr4:96548588-96548589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs72667493	chr4:96548597-96548598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571321799	chr4:96548634-96548635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144838733	chr4:96548743-96548744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554086981	chr4:96548783-96548784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529663031	chr4:96548815-96548816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573713596	chr4:96548846-96548847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549211640	chr4:96548859-96548860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556340803	chr4:96548904-96548905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375025410	chr4:96548918-96548919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368180233	chr4:96548972-96548973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576088830	chr4:96548979-96548980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544735793	chr4:96549017-96549018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192198591	chr4:96549059-96549060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564716689	chr4:96549063-96549064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533334585	chr4:96549103-96549104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571513554	chr4:96549107-96549108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560406704	chr4:96549112-96549113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185266889	chr4:96549194-96549195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148574061	chr4:96549235-96549236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96544000-96549000	Weak transcription	Aorta	Aorta
2	chr4:96547200-96549000	Weak transcription	Fetal Stomach	stomach
3	chr4:96548200-96549000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:96548600-96550400	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr4:96548800-96549000	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr4:96548800-96549400	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr4:96548800-96550600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr4:96549000-96549200	Enhancers	Fetal Stomach	stomach
9	chr4:96549000-96549400	Enhancers	Adipose Nuclei	Adipose
10	chr4:96549000-96549400	Enhancers	Aorta	Aorta
11	chr4:96549000-96550000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr4:96549400-96549800	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr4:96549600-96550400	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr4:96549600-96550400	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr4:96549800-96550400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr4:96550000-96550400	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr4:96550000-96550600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr4:96550200-96550600	Enhancers	H9 Cell Line	embryonic stem cell
19	chr4:96550400-96560000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr4:96557800-96558200	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr4:96557800-96558600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr4:96557800-96558600	Enhancers	Brain Substantia Nigra	brain
23	chr4:96558000-96558200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:96558000-96558400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr4:96558000-96558600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr4:96558000-96558600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr4:96558000-96558600	Enhancers	Fetal Stomach	stomach
28	chr4:96558200-96558400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr4:96558200-96558600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr4:96558200-96558600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr4:96558200-96558600	Enhancers	Brain Anterior Caudate	brain
32	chr4:96558200-96558600	Enhancers	Brain Cingulate Gyrus	brain
33	chr4:96558200-96561600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:96558400-96558600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr4:96558400-96558600	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr4:96558400-96558600	Enhancers	HMEC	breast
37	chr4:96558400-96561800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr4:96558600-96559600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr4:96558600-96559800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr4:96558600-96559800	Weak transcription	Brain Cingulate Gyrus	brain
41	chr4:96558600-96560000	Weak transcription	Brain Substantia Nigra	brain
42	chr4:96558600-96560200	Weak transcription	Brain Anterior Caudate	brain
43	chr4:96558600-96560200	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr4:96558600-96560400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr4:96558600-96561600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr4:96558600-96561800	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr4:96558600-96561800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr4:96558600-96561800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr4:96558800-96560000	Weak transcription	HMEC	breast
50	chr4:96559200-96559800	Enhancers	Dnd41	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links