Variant report

Variant	esv3384771
Chromosome Location	chr6:101996253-102283808
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	chr6:102056602-102056963	HepG2	liver:	n/a	n/a
2	BACH1	chr6:102045581-102045848	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:102190092-102190181	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr6:102254089-102254353	GM12878	blood:	n/a	n/a
5	BATF	chr6:102254134-102254370	GM12878	blood:	n/a	n/a
6	BATF	chr6:102053735-102054095	GM12878	blood:	n/a	n/a
7	BATF	chr6:102053779-102054143	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:102164743-102165145	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr6:102053790-102054092	GM12878	blood:	n/a	n/a
10	BCL11A	chr6:102062798-102062989	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr6:102053843-102054122	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:102126920-102126952	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:102278474-102278651	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:102099482-102099484	GM12878	blood:	n/a	n/a
15	BRCA1	chr6:102199591-102199657	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr6:102209176-102209575	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr6:102053768-102054276	HCT-116	colon:	n/a	n/a
18	CBX3	chr6:102062519-102063174	HCT-116	colon:	n/a	chr6:102063060-102063071
19	CBX3	chr6:102062577-102063026	HCT-116	colon:	n/a	n/a
20	CCNT2	chr6:102021902-102022045	K562	blood:	n/a	n/a
21	CEBPB	chr6:102209082-102209577	MCF-7	breast:	n/a	chr6:102209320-102209331 chr6:102209416-102209429 chr6:102209416-102209429 chr6:102209417-102209428 chr6:102209320-102209333 chr6:102209416-102209427 chr6:102209320-102209331 chr6:102209416-102209427
22	CEBPB	chr6:102274727-102274964	A549	lung:	n/a	chr6:102274824-102274835 chr6:102274826-102274837 chr6:102274826-102274835
23	CEBPB	chr6:102209367-102209406	K562	blood:	n/a	n/a
24	CEBPB	chr6:102227170-102227435	A549	lung:	n/a	chr6:102227346-102227359 chr6:102227348-102227357 chr6:102227348-102227359 chr6:102227346-102227357 chr6:102227346-102227359 chr6:102227346-102227359 chr6:102227348-102227357 chr6:102227348-102227359 chr6:102227348-102227357 chr6:102227366-102227377 chr6:102227348-102227357
25	CEBPB	chr6:102203529-102203786	HepG2	liver:	n/a	chr6:102203667-102203680 chr6:102203668-102203679
26	CEBPB	chr6:102153754-102154107	IMR90	lung:	n/a	n/a
27	CEBPB	chr6:102195642-102195930	IMR90	lung:	n/a	chr6:102195743-102195754
28	CEBPB	chr6:102166623-102166889	HepG2	liver:	n/a	chr6:102166758-102166767 chr6:102166758-102166767 chr6:102166756-102166767 chr6:102166758-102166767 chr6:102166757-102166768 chr6:102166758-102166767 chr6:102166756-102166769
29	CEBPB	chr6:102086438-102087046	A549	lung:	n/a	chr6:102086970-102086981
30	CEBPB	chr6:102062640-102063157	HCT-116	colon:	n/a	n/a
31	CEBPB	chr6:102166598-102166894	IMR90	lung:	n/a	chr6:102166758-102166767 chr6:102166758-102166767 chr6:102166756-102166767 chr6:102166758-102166767 chr6:102166757-102166768 chr6:102166758-102166767 chr6:102166756-102166769
32	CEBPB	chr6:102226957-102227511	IMR90	lung:	n/a	chr6:102227346-102227359 chr6:102227348-102227357 chr6:102227348-102227359 chr6:102227346-102227357 chr6:102227346-102227359 chr6:102227346-102227359 chr6:102227348-102227357 chr6:102227348-102227359 chr6:102227348-102227357 chr6:102227366-102227377 chr6:102227348-102227357
33	CEBPB	chr6:102219686-102219951	A549	lung:	n/a	n/a
34	CEBPB	chr6:102056590-102056959	HepG2	liver:	n/a	n/a
35	CEBPB	chr6:102164564-102165049	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr6:102086435-102087130	IMR90	lung:	n/a	chr6:102086970-102086981
37	CEBPB	chr6:102249097-102249352	IMR90	lung:	n/a	chr6:102249216-102249228 chr6:102249315-102249327
38	CEBPB	chr6:102171046-102171493	A549	lung:	n/a	chr6:102171310-102171327 chr6:102171313-102171326 chr6:102171325-102171338 chr6:102171322-102171339 chr6:102171313-102171326 chr6:102171313-102171326 chr6:102171315-102171326 chr6:102171315-102171326
39	CEBPB	chr6:102062818-102063063	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr6:102037169-102037304	HepG2	liver:	n/a	chr6:102037246-102037257
41	CEBPB	chr6:102045561-102046041	IMR90	lung:	n/a	n/a
42	CEBPB	chr6:102086410-102087126	HepG2	liver:	n/a	chr6:102086970-102086981
43	CEBPB	chr6:102274644-102275015	IMR90	lung:	n/a	chr6:102274824-102274835 chr6:102274826-102274837 chr6:102274826-102274835
44	CEBPB	chr6:102086613-102087169	MCF-7	breast:	n/a	chr6:102086970-102086981
45	CEBPB	chr6:102086791-102087116	H1-hESC	embryonic stem cell:	n/a	chr6:102086970-102086981
46	CEBPB	chr6:102274656-102275007	HepG2	liver:	n/a	chr6:102274824-102274835 chr6:102274826-102274837 chr6:102274826-102274835
47	CEBPB	chr6:102037085-102037425	HepG2	liver:	n/a	chr6:102037246-102037257
48	CEBPB	chr6:102209296-102209605	HepG2	liver:	n/a	chr6:102209320-102209331 chr6:102209416-102209429 chr6:102209416-102209429 chr6:102209417-102209428 chr6:102209320-102209333 chr6:102209416-102209427 chr6:102209320-102209331 chr6:102209416-102209427
49	CEBPB	chr6:102062489-102063215	HCT-116	colon:	n/a	n/a
50	CEBPB	chr6:102209123-102209656	IMR90	lung:	n/a	chr6:102209320-102209331 chr6:102209416-102209429 chr6:102209416-102209429 chr6:102209417-102209428 chr6:102209320-102209333 chr6:102209416-102209427 chr6:102209320-102209331 chr6:102209416-102209427

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:102062733-102062783	MCF10A-Er-Src	breast:	n/a
2	chr6:102062733-102062783	PFSK-1	brain:	n/a
3	chr6:102055059-102055109	ovcar-3	ovarian:	n/a
4	chr6:102062733-102062783	GM12891	blood:	n/a
5	chr6:102098727-102098777	HL-60	blood:	n/a
6	chr6:102166512-102166562	BE2_C	brain:	n/a
7	chr6:102088363-102088413	AG04450	lung:	fetal
8	chr6:102188078-102188128	Hela-S3	cervix:	n/a
9	chr6:102055059-102055109	MCF-7	breast:	n/a
10	chr6:102062733-102062783	SK-N-SH	brain:	n/a
11	chr6:102062733-102062783	GM06990	blood:	n/a
12	chr6:102224868-102224918	A549	lung:	n/a
13	chr6:102224868-102224918	PANC-1	pancreas:	n/a
14	chr6:102166512-102166562	PrEC	prostate:	n/a
15	chr6:102224868-102224918	Caco-2	colon:	n/a
16	chr6:102098727-102098777	BJ	skin:	n/a
17	chr6:102166512-102166562	HCT-116	colon:	n/a
18	chr6:102055059-102055109	HNPCEpiC	eye:	n/a
19	chr6:102166512-102166562	PANC-1	pancreas:	n/a
20	chr6:102115051-102115101	LNCaP	prostate:	n/a
21	chr6:102088363-102088413	SK-N-SH_RA	brain:	n/a
22	chr6:102188078-102188128	HL-60	blood:	n/a
23	chr6:102115051-102115101	T-47D	breast:	n/a
24	chr6:102062733-102062783	NB4	blood:	n/a
25	chr6:102055059-102055109	Caco-2	colon:	n/a
26	chr6:102088363-102088413	MCF10A-Er-Src	breast:	n/a
27	chr6:102088363-102088413	AoSMC	blood vessel:	n/a
28	chr6:102098727-102098777	HRPEpiC	eye:	n/a
29	chr6:102115051-102115101	AG04449	skin:	fetal
30	chr6:102088363-102088413	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:102149251-102149301	SK-N-MC	brain:	n/a
32	chr6:102224868-102224918	AG09319	gingival:	n/a
33	chr6:102098727-102098777	A549	lung:	n/a
34	chr6:102242072-102242122	PFSK-1	brain:	n/a
35	chr6:102098727-102098777	HAEpiC	amniotic membrane:	n/a
36	chr6:102115051-102115101	RPTEC	kidney:	n/a
37	chr6:102242072-102242122	U87	brain:	n/a
38	chr6:102088363-102088413	HUVEC	blood vessel:	n/a
39	chr6:102224868-102224918	RPTEC	kidney:	n/a
40	chr6:102055059-102055109	HRPEpiC	eye:	n/a
41	chr6:102166512-102166562	HCM	heart:	n/a
42	chr6:102242072-102242122	SK-N-MC	brain:	n/a
43	chr6:102166512-102166562	Jurkat	blood:	n/a
44	chr6:102055059-102055109	AG10803	skin:	n/a
45	chr6:102062733-102062783	ProgFib	skin:	n/a
46	chr6:102055059-102055109	HCM	heart:	n/a
47	chr6:102055059-102055109	SAEC	small airway:	n/a
48	chr6:102149251-102149301	HCF	heart:	n/a
49	chr6:102242072-102242122	GM06990	blood:	n/a
50	chr6:102242072-102242122	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:102014386..102015979-chr6:102018892..102021029,2	K562	blood:
2	chr6:102000178..102002016-chr6:102006713..102008443,2	K562	blood:
3	chr6:102028266..102030004-chr6:102035666..102038044,2	K562	blood:
4	chr6:102014386..102015979-chr6:102018892..102021029,2	K562	blood:
5	chr6:102198814..102201374-chr6:102217508..102220238,2	K562	blood:
6	chr6:102241098..102243471-chr6:102247129..102249278,2	K562	blood:
7	chr6:102270226..102272890-chr6:102273538..102276140,2	K562	blood:
8	chr6:102153395..102155355-chr6:102159822..102161608,2	K562	blood:
9	chr6:102173348..102176230-chr6:102178653..102180675,2	K562	blood:
10	chr6:102270226..102272890-chr6:102273538..102276140,2	K562	blood:
11	chr6:102173348..102176230-chr6:102178653..102180675,2	K562	blood:
12	chr3:61667747..61668495-chr6:102049744..102050312,2	MCF-7	breast:
13	chr6:102241098..102243471-chr6:102247129..102249278,2	K562	blood:
14	chr6:102198814..102201374-chr6:102217508..102220238,2	K562	blood:
15	chr6:101845030..101845934-chr6:102093542..102094670,3	MCF-7	breast:
16	chr6:102066602..102069152-chr6:102074799..102076999,2	MCF-7	breast:
17	chr6:102153395..102155355-chr6:102159822..102161608,2	K562	blood:
18	chr6:102000178..102002016-chr6:102006713..102008443,2	K562	blood:
19	chr6:102028266..102030004-chr6:102035666..102038044,2	K562	blood:

Variant related genes	Relation type
GRIK2	TF binding region
GRIK2	CpG island
ENSG00000164418	chromatin interactions

Extended variants
information (count: 7665 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:7665 , 50 per page) page: 1 2 3 4 5 6 7 ... 154

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189767129	chr6:101996278-101996279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs9322598	chr6:101996322-101996323	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs541159919	chr6:101996333-101996334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559505602	chr6:101996336-101996337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533031552	chr6:101996370-101996371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545188828	chr6:101996371-101996372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181465162	chr6:101996390-101996391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557764928	chr6:101996404-101996405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530872814	chr6:101996447-101996448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549002437	chr6:101996456-101996457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568146404	chr6:101996464-101996465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs578239860	chr6:101996465-101996466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529236198	chr6:101996469-101996470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115169662	chr6:101996472-101996473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186057827	chr6:101996507-101996508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140995018	chr6:101996522-101996523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577683029	chr6:101996529-101996530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558340204	chr6:101996549-101996550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570141553	chr6:101996551-101996552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537796811	chr6:101996555-101996556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537064189	chr6:101996557-101996558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556078034	chr6:101996564-101996565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574348291	chr6:101996571-101996572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541049219	chr6:101996586-101996587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557726418	chr6:101996594-101996595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs57520191	chr6:101996595-101996596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544765757	chr6:101996629-101996630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189011112	chr6:101996674-101996675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575322557	chr6:101996687-101996688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371497891	chr6:101996690-101996691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147828474	chr6:101996709-101996710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2749075	chr6:101996719-101996720	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs141370213	chr6:101996731-101996732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs199913703	chr6:101996746-101996747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547393452	chr6:101996780-101996781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559281940	chr6:101996804-101996805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533509047	chr6:101996829-101996830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551581715	chr6:101996950-101996951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201336984	chr6:101996961-101996962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs180854247	chr6:101996988-101996989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2749074	chr6:101997051-101997052	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs372987837	chr6:101997067-101997068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549570221	chr6:101997073-101997074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567963083	chr6:101997112-101997113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372027850	chr6:101997151-101997152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76548818	chr6:101997152-101997153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs72398338	chr6:101997163-101997164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76758189	chr6:101997164-101997165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34763570	chr6:101997165-101997166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201233263	chr6:101997166-101997167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17170743	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Obesity	21045960	CNVD
Liver carcinoma	19366792	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	22543975	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:723 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:101991600-102001600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr6:101998600-101999400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:101999400-102000000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:101999800-102000600	Enhancers	Ovary	ovary
5	chr6:102000000-102000200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:102000200-102003000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:102000600-102001200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr6:102001600-102002000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:102001800-102002000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:102001800-102002400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr6:102001800-102002600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr6:102001800-102002800	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr6:102001800-102003200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr6:102002000-102003000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:102002000-102003400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr6:102002000-102004600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr6:102002400-102003000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr6:102002600-102003600	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr6:102003000-102003200	Enhancers	H1 Cell Line	embryonic stem cell
20	chr6:102003000-102003400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr6:102003000-102003400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr6:102003400-102004400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:102003800-102004000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr6:102004400-102006200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr6:102004600-102006000	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr6:102006000-102006200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr6:102006200-102010600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr6:102018000-102018200	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr6:102018400-102018800	Enhancers	H1 Cell Line	embryonic stem cell
30	chr6:102021200-102021600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr6:102030400-102031200	Enhancers	Brain Substantia Nigra	brain
32	chr6:102030600-102031200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:102030600-102031400	Enhancers	Brain Angular Gyrus	brain
34	chr6:102030600-102031800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr6:102030800-102031600	Enhancers	Brain Hippocampus Middle	brain
36	chr6:102030800-102031600	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr6:102031200-102031600	Flanking Active TSS	Brain Substantia Nigra	brain
38	chr6:102031200-102031800	Enhancers	Brain Cingulate Gyrus	brain
39	chr6:102036000-102036600	Enhancers	Fetal Heart	heart
40	chr6:102036600-102040800	Weak transcription	Fetal Heart	heart
41	chr6:102040800-102042200	Enhancers	Fetal Heart	heart
42	chr6:102041400-102041600	Enhancers	Rectal Smooth Muscle	rectum
43	chr6:102042200-102042400	Enhancers	Rectal Smooth Muscle	rectum
44	chr6:102043000-102043200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr6:102043000-102043400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr6:102043000-102044000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr6:102043200-102043400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr6:102043400-102044000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr6:102043400-102045400	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr6:102044000-102045400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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