Variant report

Variant	esv1819438
Chromosome Location	chr6:102211675-102279200
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	BATF	chr6:102254134-102254370	GM12878	blood:	n/a	n/a
2	BATF	chr6:102254089-102254353	GM12878	blood:	n/a	n/a
3	BHLHE40	chr6:102278474-102278651	GM12878	blood:	n/a	n/a
4	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
5	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
6	CEBPB	chr6:102219713-102219913	HepG2	liver:	n/a	n/a
7	CEBPB	chr6:102274680-102274946	H1-hESC	embryonic stem cell:	n/a	chr6:102274824-102274835 chr6:102274826-102274837 chr6:102274826-102274835
8	CEBPB	chr6:102219709-102219953	IMR90	lung:	n/a	n/a
9	CEBPB	chr6:102274656-102275007	HepG2	liver:	n/a	chr6:102274824-102274835 chr6:102274826-102274837 chr6:102274826-102274835
10	CEBPB	chr6:102274644-102275015	IMR90	lung:	n/a	chr6:102274824-102274835 chr6:102274826-102274837 chr6:102274826-102274835
11	CEBPB	chr6:102227182-102227513	HepG2	liver:	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
12	CEBPB	chr6:102274727-102274964	A549	lung:	n/a	chr6:102274824-102274835 chr6:102274826-102274837 chr6:102274826-102274835
13	CEBPB	chr6:102226991-102227552	Hela-S3	cervix:	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
14	CEBPB	chr6:102249097-102249352	IMR90	lung:	n/a	chr6:102249216-102249228 chr6:102249315-102249327
15	CEBPB	chr6:102219686-102219951	A549	lung:	n/a	n/a
16	CEBPB	chr6:102227290-102227479	H1-hESC	embryonic stem cell:	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
17	CTCF	chr6:102230462-102230502	Medullo	brain:	n/a	n/a
18	CTCF	chr6:102255040-102255190	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr6:102271818-102271890	GM10248	blood:	n/a	n/a
20	CTCF	chr6:102235594-102235662	GM13976	blood:	n/a	n/a
21	CTCF	chr6:102232726-102232767	GM13977	blood:	n/a	n/a
22	E2F4	chr6:102214677-102214877	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr6:102235381-102235620	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr6:102227046-102227345	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr6:102270125-102270408	MCF10A-Er-Src	breast:	n/a	n/a
26	EBF1	chr6:102278591-102278648	GM12878	blood:	n/a	n/a
27	EBF1	chr6:102231022-102231241	GM12878	blood:	n/a	n/a
28	EP300	chr6:102253962-102254787	SK-N-SH	brain:	n/a	chr6:102254120-102254134
29	EP300	chr6:102253891-102254671	SK-N-SH	brain:	n/a	chr6:102254120-102254134
30	EP300	chr6:102254085-102254477	SK-N-SH_RA	brain:	n/a	chr6:102254120-102254134
31	EP300	chr6:102251052-102251444	SK-N-SH	brain:	n/a	n/a
32	EP300	chr6:102254044-102254481	SK-N-SH_RA	brain:	n/a	chr6:102254120-102254134
33	FOS	chr6:102217934-102218136	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr6:102217886-102218145	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr6:102226938-102227363	MCF10A-Er-Src	breast:	n/a	chr6:102227102-102227112
36	FOS	chr6:102217857-102218153	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr6:102217864-102218174	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr6:102226947-102227294	MCF10A-Er-Src	breast:	n/a	chr6:102227102-102227112
39	FOS	chr6:102278747-102278756	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr6:102266391-102266504	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr6:102226938-102227314	MCF10A-Er-Src	breast:	n/a	chr6:102227102-102227112
42	FOS	chr6:102253867-102254879	HUVEC	blood vessel:	n/a	n/a
43	FOS	chr6:102226939-102227339	MCF10A-Er-Src	breast:	n/a	chr6:102227102-102227112
44	FOSL2	chr6:102251008-102251481	SK-N-SH	brain:	n/a	chr6:102251286-102251297 chr6:102251285-102251293 chr6:102251283-102251295 chr6:102251285-102251292
45	FOSL2	chr6:102253891-102254683	SK-N-SH	brain:	n/a	n/a
46	FOXA1	chr6:102241643-102241922	HepG2	liver:	n/a	n/a
47	FOXA2	chr6:102241561-102242107	A549	lung:	n/a	n/a
48	GATA2	chr6:102253957-102254711	HUVEC	blood vessel:	n/a	chr6:102254537-102254553 chr6:102254114-102254124 chr6:102254537-102254553 chr6:102254540-102254550
49	GATA3	chr6:102258850-102259290	SK-N-SH	brain:	n/a	n/a
50	GATA3	chr6:102258878-102259383	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:102242072-102242122	GM12878	blood:	n/a
2	chr6:102224868-102224918	HCT-116	colon:	n/a
3	chr6:102224868-102224918	AG04449	skin:	fetal
4	chr6:102224868-102224918	HepG2	liver:	n/a
5	chr6:102224868-102224918	NHDF-neo	bronchial:	n/a
6	chr6:102224868-102224918	SKMC	muscle:	n/a
7	chr6:102224868-102224918	PFSK-1	brain:	n/a
8	chr6:102224868-102224918	CMK	blood:	n/a
9	chr6:102224868-102224918	Hela-S3	cervix:	n/a
10	chr6:102242072-102242122	U87	brain:	n/a
11	chr6:102242072-102242122	AG04449	skin:	fetal
12	chr6:102224868-102224918	HCF	heart:	n/a
13	chr6:102242072-102242122	GM12892	blood:	n/a
14	chr6:102224868-102224918	SK-N-SH_RA	brain:	n/a
15	chr6:102242072-102242122	K562	blood:	n/a
16	chr6:102242072-102242122	HNPCEpiC	eye:	n/a
17	chr6:102242072-102242122	AoSMC	blood vessel:	n/a
18	chr6:102224868-102224918	HRE	kidney:	n/a
19	chr6:102224868-102224918	GM19239	blood:	n/a
20	chr6:102224868-102224918	HPAEpiC	pulmonary alveolar:	n/a
21	chr6:102242072-102242122	HEEpiC	esophagus:	n/a
22	chr6:102242072-102242122	AG04450	lung:	fetal
23	chr6:102242072-102242122	HIPEpiC	eye:	n/a
24	chr6:102242072-102242122	HRCEpiC	kidney:	n/a
25	chr6:102242072-102242122	AG09319	gingival:	n/a
26	chr6:102242072-102242122	NB4	blood:	n/a
27	chr6:102242072-102242122	Jurkat	blood:	n/a
28	chr6:102224868-102224918	ECC-1	luminal epithelium:	n/a
29	chr6:102224868-102224918	NH-A	brain:	n/a
30	chr6:102224868-102224918	SK-N-SH	brain:	n/a
31	chr6:102224868-102224918	Hepatocyte	liver:	n/a
32	chr6:102242072-102242122	CMK	blood:	n/a
33	chr6:102224868-102224918	IMR90	lung:	fetal
34	chr6:102242072-102242122	ECC-1	luminal epithelium:	n/a
35	chr6:102224868-102224918	GM12892	blood:	n/a
36	chr6:102242072-102242122	Hela-S3	cervix:	n/a
37	chr6:102242072-102242122	MCF-7	breast:	n/a
38	chr6:102242072-102242122	AG10803	skin:	n/a
39	chr6:102224868-102224918	AG09309	skin:	n/a
40	chr6:102242072-102242122	HEK293	kidney:	embryo
41	chr6:102224868-102224918	Jurkat	blood:	n/a
42	chr6:102224868-102224918	HEK293	kidney:	embryo
43	chr6:102242072-102242122	HRE	kidney:	n/a
44	chr6:102242072-102242122	GM06990	blood:	n/a
45	chr6:102242072-102242122	SK-N-MC	brain:	n/a
46	chr6:102242072-102242122	HCPEpiC	choroid plexus:	n/a
47	chr6:102224868-102224918	NB4	blood:	n/a
48	chr6:102242072-102242122	ProgFib	skin:	n/a
49	chr6:102242072-102242122	SK-N-SH	brain:	n/a
50	chr6:102224868-102224918	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:102270226..102272890-chr6:102273538..102276140,2	K562	blood:
2	chr6:102198814..102201374-chr6:102217508..102220238,2	K562	blood:
3	chr6:102241098..102243471-chr6:102247129..102249278,2	K562	blood:
4	chr6:102241098..102243471-chr6:102247129..102249278,2	K562	blood:
5	chr6:102270226..102272890-chr6:102273538..102276140,2	K562	blood:

Variant related genes	Relation type
GRIK2	TF binding region
GRIK2	CpG island

Extended variants
information (count: 2051 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:2051 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7749469	chr6:102211675-102211676	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565880623	chr6:102211677-102211678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539425833	chr6:102211680-102211681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557763741	chr6:102211687-102211688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530910471	chr6:102211700-102211701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576292541	chr6:102211708-102211709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs200924339	chr6:102211716-102211717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185615048	chr6:102211728-102211729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542829855	chr6:102211756-102211757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555882830	chr6:102211784-102211785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150764609	chr6:102211802-102211803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9498691	chr6:102211817-102211818	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs115267290	chr6:102211842-102211843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34133340	chr6:102211858-102211859	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs77113933	chr6:102211859-102211860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138096737	chr6:102211870-102211871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143113750	chr6:102211940-102211941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564961206	chr6:102211953-102211954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114552543	chr6:102212027-102212028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549014787	chr6:102212058-102212059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190703753	chr6:102212064-102212065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs80226065	chr6:102212088-102212089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564766352	chr6:102212097-102212098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546416918	chr6:102212108-102212109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs78129943	chr6:102212124-102212125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs9377300	chr6:102212160-102212161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377413453	chr6:102212168-102212169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76414472	chr6:102212265-102212266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77298774	chr6:102212270-102212271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567451274	chr6:102212281-102212282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569719783	chr6:102212295-102212296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200203857	chr6:102212319-102212320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs75991539	chr6:102212320-102212321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187161439	chr6:102212325-102212326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs144599253	chr6:102212326-102212327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192089397	chr6:102212327-102212328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534886705	chr6:102212328-102212329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553640052	chr6:102212429-102212430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142699504	chr6:102212497-102212498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545149037	chr6:102212499-102212500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73512722	chr6:102212593-102212594	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs548454932	chr6:102212611-102212612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373983917	chr6:102212632-102212633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs73761417	chr6:102212642-102212643	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs113545406	chr6:102212715-102212716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs9498692	chr6:102212718-102212719	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs374654446	chr6:102212722-102212723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534847234	chr6:102212748-102212749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183459251	chr6:102212749-102212750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs561000795	chr6:102212767-102212768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:102207400-102217800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr6:102207600-102212200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr6:102207600-102212800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr6:102208600-102211800	Enhancers	Liver	Liver
5	chr6:102209200-102213000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr6:102209200-102214400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr6:102209200-102217000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:102209400-102214400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr6:102210800-102214000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:102211200-102212600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr6:102211200-102212800	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr6:102211200-102212800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr6:102211200-102213000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr6:102211200-102213000	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr6:102211800-102212800	Weak transcription	Liver	Liver
16	chr6:102212000-102212200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr6:102212200-102212800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:102212200-102215200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr6:102212600-102214400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr6:102212800-102213000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr6:102212800-102213000	Enhancers	Liver	Liver
22	chr6:102212800-102213400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr6:102212800-102213800	Enhancers	H9 Cell Line	embryonic stem cell
24	chr6:102212800-102215000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr6:102212800-102215800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr6:102213000-102213400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr6:102213000-102215200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr6:102213000-102215400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr6:102213000-102215400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr6:102213000-102216200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr6:102213400-102217400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr6:102213800-102214200	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr6:102214200-102214800	Enhancers	H9 Cell Line	embryonic stem cell
34	chr6:102214400-102215000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr6:102214400-102215000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr6:102214400-102215200	Enhancers	H1 Cell Line	embryonic stem cell
37	chr6:102214800-102224800	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr6:102215000-102215200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr6:102215000-102217600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr6:102215200-102217000	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr6:102215200-102217000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr6:102215200-102217600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr6:102215200-102217600	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr6:102215400-102217000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr6:102215400-102217600	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr6:102215800-102217600	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr6:102216200-102216400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr6:102217000-102218200	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr6:102217000-102218400	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr6:102217000-102218600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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