Variant report

Variant	nsv879681
Chromosome Location	chr4:102641265-102769677
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	chr4:102651772-102651979	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:102695953-102696345	HepG2	liver:	n/a	n/a
3	ATF2	chr4:102727996-102728516	GM12878	blood:	n/a	n/a
4	ATF2	chr4:102727971-102728551	GM12878	blood:	n/a	n/a
5	ATF2	chr4:102711518-102712077	GM12878	blood:	n/a	n/a
6	ATF2	chr4:102711410-102712088	GM12878	blood:	n/a	n/a
7	BATF	chr4:102728054-102728394	GM12878	blood:	n/a	chr4:102728254-102728263
8	BATF	chr4:102713427-102713837	GM12878	blood:	n/a	chr4:102713504-102713512
9	BATF	chr4:102713420-102713648	GM12878	blood:	n/a	chr4:102713504-102713512
10	BATF	chr4:102711635-102711995	GM12878	blood:	n/a	n/a
11	BATF	chr4:102703727-102703964	GM12878	blood:	n/a	chr4:102703836-102703847
12	BATF	chr4:102651652-102651967	GM12878	blood:	n/a	n/a
13	BATF	chr4:102728011-102728377	GM12878	blood:	n/a	chr4:102728254-102728263
14	BCL11A	chr4:102728103-102728355	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:102711669-102711979	GM12878	blood:	n/a	chr4:102711814-102711823 chr4:102711945-102711954
16	BCL11A	chr4:102728040-102728390	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:102711557-102711983	GM12878	blood:	n/a	chr4:102711814-102711823 chr4:102711945-102711954
18	BCL3	chr4:102711691-102711970	GM12878	blood:	n/a	chr4:102711814-102711823 chr4:102711945-102711954
19	BCL3	chr4:102728039-102728486	GM12878	blood:	n/a	n/a
20	BCL3	chr4:102711661-102712049	GM12878	blood:	n/a	chr4:102711814-102711823 chr4:102711945-102711954
21	BCLAF1	chr4:102711441-102712085	GM12878	blood:	n/a	chr4:102711814-102711823 chr4:102711945-102711954
22	BCLAF1	chr4:102711548-102712021	GM12878	blood:	n/a	chr4:102711814-102711823 chr4:102711945-102711954
23	BHLHE40	chr4:102728061-102728467	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:102645420-102645722	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:102711628-102712010	GM12878	blood:	n/a	chr4:102711991-102712007
26	BHLHE40	chr4:102728731-102728861	GM12878	blood:	n/a	n/a
27	BRCA1	chr4:102678590-102678637	GM12878	blood:	n/a	n/a
28	BRCA1	chr4:102756835-102756998	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr4:102651391-102652158	HCT-116	colon:	n/a	n/a
30	CBX3	chr4:102692873-102693335	HCT-116	colon:	n/a	n/a
31	CEBPB	chr4:102768673-102768756	HepG2	liver:	n/a	chr4:102768710-102768721
32	CEBPB	chr4:102674884-102675289	MCF-7	breast:	n/a	chr4:102675081-102675090 chr4:102675081-102675090 chr4:102675081-102675090 chr4:102675081-102675090
33	CEBPB	chr4:102716927-102717201	ECC-1	luminal epithelium:	n/a	chr4:102717046-102717057 chr4:102717066-102717077
34	CEBPB	chr4:102749628-102749901	A549	lung:	n/a	chr4:102749720-102749731
35	CEBPB	chr4:102715532-102715637	HepG2	liver:	n/a	chr4:102715573-102715584
36	CEBPB	chr4:102757978-102758176	A549	lung:	n/a	chr4:102757983-102757994
37	CEBPB	chr4:102745784-102746488	HepG2	liver:	n/a	chr4:102745904-102745917 chr4:102745904-102745917 chr4:102745904-102745915 chr4:102746333-102746344
38	CEBPB	chr4:102749634-102749897	HepG2	liver:	n/a	chr4:102749720-102749731
39	CEBPB	chr4:102756505-102757162	HCT-116	colon:	n/a	chr4:102756836-102756849
40	CEBPB	chr4:102756617-102757041	Hela-S3	cervix:	n/a	chr4:102756836-102756849
41	CEBPB	chr4:102756691-102757013	HepG2	liver:	n/a	chr4:102756836-102756849
42	CEBPB	chr4:102756667-102757029	IMR90	lung:	n/a	chr4:102756836-102756849
43	CEBPB	chr4:102763284-102763412	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr4:102756702-102757033	A549	lung:	n/a	chr4:102756836-102756849
45	CEBPB	chr4:102756649-102757104	MCF-7	breast:	n/a	chr4:102756836-102756849
46	CEBPB	chr4:102674930-102675268	Hela-S3	cervix:	n/a	chr4:102675081-102675090 chr4:102675081-102675090 chr4:102675081-102675090 chr4:102675081-102675090
47	CEBPB	chr4:102736022-102736294	IMR90	lung:	n/a	n/a
48	CEBPB	chr4:102674889-102675265	MCF-7	breast:	n/a	chr4:102675081-102675090 chr4:102675081-102675090 chr4:102675081-102675090 chr4:102675081-102675090
49	CEBPB	chr4:102745750-102746467	IMR90	lung:	n/a	chr4:102745904-102745917 chr4:102745904-102745917 chr4:102745904-102745915 chr4:102746333-102746344
50	CEBPB	chr4:102674882-102675225	ECC-1	luminal epithelium:	n/a	chr4:102675081-102675090 chr4:102675081-102675090 chr4:102675081-102675090 chr4:102675081-102675090

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:102712082-102712132	MCF10A-Er-Src	breast:	n/a
2	chr4:102745414-102745464	AG10803	skin:	n/a
3	chr4:102711773-102711823	NHBE	bronchial:	n/a
4	chr4:102711702-102711752	HCT-116	colon:	n/a
5	chr4:102709336-102709386	NT2-D1	testis:	n/a
6	chr4:102737794-102737844	T-47D	breast:	n/a
7	chr4:102711747-102711797	U87	brain:	n/a
8	chr4:102709336-102709386	HNPCEpiC	eye:	n/a
9	chr4:102715139-102715189	SK-N-SH_RA	brain:	n/a
10	chr4:102712397-102712447	PrEC	prostate:	n/a
11	chr4:102712397-102712447	GM19239	blood:	n/a
12	chr4:102737794-102737844	A549	lung:	n/a
13	chr4:102712010-102712060	HMEC	breast:	n/a
14	chr4:102737794-102737844	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:102712082-102712132	GM12878	blood:	n/a
16	chr4:102734752-102734802	AG04449	skin:	fetal
17	chr4:102737794-102737844	HUVEC	blood vessel:	n/a
18	chr4:102745414-102745464	Jurkat	blood:	n/a
19	chr4:102711702-102711752	AG09319	gingival:	n/a
20	chr4:102711702-102711752	GM19239	blood:	n/a
21	chr4:102734752-102734802	GM19239	blood:	n/a
22	chr4:102711773-102711823	AG10803	skin:	n/a
23	chr4:102711773-102711823	GM06990	blood:	n/a
24	chr4:102737794-102737844	GM12892	blood:	n/a
25	chr4:102745414-102745464	HRE	kidney:	n/a
26	chr4:102712010-102712060	SK-N-SH	brain:	n/a
27	chr4:102712397-102712447	MCF-7	breast:	n/a
28	chr4:102712010-102712060	MCF-7	breast:	n/a
29	chr4:102711773-102711823	BJ	skin:	n/a
30	chr4:102709336-102709386	Jurkat	blood:	n/a
31	chr4:102734752-102734802	HL-60	blood:	n/a
32	chr4:102712216-102712266	ECC-1	luminal epithelium:	n/a
33	chr4:102709336-102709386	SK-N-SH_RA	brain:	n/a
34	chr4:102715139-102715189	RPTEC	kidney:	n/a
35	chr4:102711702-102711752	NH-A	brain:	n/a
36	chr4:102712010-102712060	NB4	blood:	n/a
37	chr4:102734752-102734802	HNPCEpiC	eye:	n/a
38	chr4:102712216-102712266	GM19239	blood:	n/a
39	chr4:102734752-102734802	MCF-7	breast:	n/a
40	chr4:102712082-102712132	HL-60	blood:	n/a
41	chr4:102711702-102711752	AG04450	lung:	fetal
42	chr4:102734752-102734802	NHDF-neo	bronchial:	n/a
43	chr4:102709336-102709386	U87	brain:	n/a
44	chr4:102711747-102711797	NH-A	brain:	n/a
45	chr4:102712082-102712132	HepG2	liver:	n/a
46	chr4:102712216-102712266	NHBE	bronchial:	n/a
47	chr4:102712010-102712060	HCF	heart:	n/a
48	chr4:102709336-102709386	Caco-2	colon:	n/a
49	chr4:102712082-102712132	Jurkat	blood:	n/a
50	chr4:102712216-102712266	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:102739568..102742034-chr4:102748015..102750811,2	K562	blood:
2	chr4:102090452..102090967-chr4:102651453..102652195,2	MCF-7	breast:
3	chr4:102679449..102682204-chr4:102682535..102685384,2	K562	blood:
4	chr4:102705460..102706994-chr4:102708122..102710097,2	MCF-7	breast:
5	chr4:102755518..102758333-chr4:102759339..102760873,2	MCF-7	breast:
6	chr4:102739568..102742034-chr4:102748015..102750811,2	K562	blood:
7	chr4:102756033..102758603-chr4:102759128..102761662,3	MCF-7	breast:
8	chr4:102668209..102669910-chr4:102674187..102676043,2	MCF-7	breast:
9	chr4:102090091..102091062-chr4:102651393..102652212,3	MCF-7	breast:
10	chr4:102705460..102706994-chr4:102708122..102710097,2	MCF-7	breast:
11	chr4:102755518..102758333-chr4:102759339..102760873,2	MCF-7	breast:
12	chr4:102748202..102750922-chr4:102785267..102786848,2	MCF-7	breast:
13	chr1:116314786..116315654-chr4:102694925..102695632,2	MCF-7	breast:
14	chr4:102228684..102230512-chr4:102715753..102717632,2	K562	blood:
15	chr4:102668209..102669910-chr4:102674187..102676043,2	MCF-7	breast:
16	chr4:102679449..102682204-chr4:102682535..102685384,2	K562	blood:
17	chr4:102151616..102153523-chr4:102648348..102650655,2	MCF-7	breast:
18	chr4:102756033..102758603-chr4:102759128..102761662,3	MCF-7	breast:

Variant related genes	Relation type
BANK1	TF binding region
RNU6-462P	TF binding region
BANK1	CpG island
RNU6-462P	CpG island

Extended variants
information (count: 3478 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:3478 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12501586	chr4:102642012-102642013	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530233313	chr4:102642048-102642049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78729535	chr4:102642052-102642053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs548417633	chr4:102642061-102642062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12648423	chr4:102642073-102642074	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs530465735	chr4:102642094-102642095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573437437	chr4:102642117-102642118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552522171	chr4:102642139-102642140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570778245	chr4:102642173-102642174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs144116097	chr4:102642175-102642176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550303281	chr4:102642205-102642206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568618177	chr4:102642221-102642222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183801638	chr4:102642269-102642270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372274944	chr4:102642275-102642276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572285642	chr4:102642289-102642290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs12506451	chr4:102642299-102642300	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs7660525	chr4:102642344-102642345	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs575956113	chr4:102642401-102642402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs10856962	chr4:102642453-102642454	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs150682876	chr4:102642455-102642456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs116407414	chr4:102642476-102642477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373195369	chr4:102642502-102642503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12506517	chr4:102642526-102642527	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs538517530	chr4:102642535-102642536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs565614527	chr4:102642704-102642705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs138895076	chr4:102642825-102642826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556930747	chr4:102642881-102642882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs527957346	chr4:102642904-102642905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531125351	chr4:102642958-102642959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368058422	chr4:102642986-102642987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577705539	chr4:102643064-102643065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564458967	chr4:102643075-102643076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531735704	chr4:102643076-102643077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs550240524	chr4:102643098-102643099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs144780302	chr4:102643156-102643157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535984860	chr4:102643168-102643169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547544043	chr4:102643170-102643171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369113003	chr4:102643185-102643186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530823077	chr4:102643195-102643196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs28523914	chr4:102643196-102643197	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs539680485	chr4:102643256-102643257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187891736	chr4:102643267-102643268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569660481	chr4:102643289-102643290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548755930	chr4:102643294-102643295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536638268	chr4:102643307-102643308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs56996820	chr4:102643320-102643321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191849619	chr4:102643395-102643396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs34872480	chr4:102643396-102643397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12643886	chr4:102643397-102643398	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs572561033	chr4:102643423-102643424	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	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
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:102642000-102643800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr4:102645000-102645800	Enhancers	Primary B cells from peripheral blood	blood
3	chr4:102645200-102645600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr4:102645200-102645600	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr4:102645200-102645600	Active TSS	Duodenum Mucosa	Duodenum
6	chr4:102645200-102645600	Active TSS	Rectal Mucosa Donor 29	rectum
7	chr4:102645200-102645800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr4:102645200-102645800	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr4:102645400-102645800	Active TSS	Gastric	stomach
10	chr4:102645400-102645800	Enhancers	Sigmoid Colon	Sigmoid Colon
11	chr4:102645800-102651200	Weak transcription	Primary B cells from peripheral blood	blood
12	chr4:102651200-102652200	Enhancers	Primary B cells from peripheral blood	blood
13	chr4:102651600-102652200	Enhancers	A549	lung
14	chr4:102651800-102652200	Enhancers	Stomach Mucosa	stomach
15	chr4:102654600-102655000	Enhancers	Adipose Nuclei	Adipose
16	chr4:102654600-102655800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:102667800-102669600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:102668000-102668200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
19	chr4:102668200-102669800	Enhancers	Primary B cells from peripheral blood	blood
20	chr4:102669400-102669800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:102674200-102674800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:102674600-102675600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr4:102674800-102675400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr4:102675400-102675600	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr4:102675600-102682600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr4:102677600-102677800	Enhancers	Primary B cells from peripheral blood	blood
27	chr4:102677800-102682800	Weak transcription	Primary B cells from peripheral blood	blood
28	chr4:102682400-102682600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr4:102682400-102682600	Enhancers	Adipose Nuclei	Adipose
30	chr4:102682400-102683200	Enhancers	Placenta	Placenta
31	chr4:102682600-102682800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr4:102682600-102682800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr4:102682600-102682800	Enhancers	Fetal Muscle Trunk	muscle
34	chr4:102682600-102683000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr4:102682600-102683000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr4:102682600-102683400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr4:102682600-102683600	Flanking Active TSS	Adipose Nuclei	Adipose
38	chr4:102682800-102683200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr4:102682800-102683200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr4:102682800-102683200	Enhancers	Primary B cells from peripheral blood	blood
41	chr4:102682800-102683200	Enhancers	Esophagus	oesophagus
42	chr4:102682800-102683400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr4:102682800-102683400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr4:102682800-102683600	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr4:102682800-102683600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr4:102683000-102683200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr4:102683000-102683400	Enhancers	Duodenum Mucosa	Duodenum
48	chr4:102683000-102683400	Active TSS	Osteobl	bone
49	chr4:102683200-102683400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr4:102683400-102683600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links