Variant report

Variant	esv2759442
Chromosome Location	chr6:74961996-75162222
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	CBX3	chr6:75053493-75053926	HCT-116	colon:	n/a	n/a
2	CBX3	chr6:75076273-75076707	HCT-116	colon:	n/a	n/a
3	CEBPB	chr6:75056353-75056636	IMR90	lung:	n/a	chr6:75056490-75056501 chr6:75056489-75056502 chr6:75056489-75056502 chr6:75056489-75056502
4	CEBPB	chr6:75161160-75161372	A549	lung:	n/a	n/a
5	CEBPB	chr6:74999604-75000012	IMR90	lung:	n/a	chr6:74999810-74999827
6	CEBPB	chr6:74963070-74963400	MCF-7	breast:	n/a	n/a
7	CEBPB	chr6:75079490-75079803	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr6:75125779-75125838	K562	blood:	n/a	n/a
9	CEBPB	chr6:74973756-74973764	HepG2	liver:	n/a	n/a
10	CEBPB	chr6:75079641-75079699	A549	lung:	n/a	n/a
11	CEBPB	chr6:75124849-75125136	IMR90	lung:	n/a	chr6:75124966-75124979
12	CEBPB	chr6:75056246-75056651	HepG2	liver:	n/a	chr6:75056490-75056501 chr6:75056489-75056502 chr6:75056489-75056502 chr6:75056489-75056502
13	CEBPB	chr6:75079170-75079922	IMR90	lung:	n/a	n/a
14	CEBPB	chr6:75056405-75056627	A549	lung:	n/a	chr6:75056490-75056501 chr6:75056489-75056502 chr6:75056489-75056502 chr6:75056489-75056502
15	CEBPB	chr6:75156805-75157005	A549	lung:	n/a	n/a
16	CEBPB	chr6:75157566-75157751	IMR90	lung:	n/a	n/a
17	CEBPB	chr6:75124885-75125040	A549	lung:	n/a	chr6:75124966-75124979
18	CEBPB	chr6:75067143-75067433	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr6:75161042-75161371	IMR90	lung:	n/a	n/a
20	CEBPB	chr6:75078501-75078804	IMR90	lung:	n/a	n/a
21	CEBPZ	chr6:74985570-74985693	HepG2	liver:	n/a	n/a
22	CHD1	chr6:75156251-75156266	GM12878	blood:	n/a	n/a
23	CHD2	chr6:75156867-75157036	GM12878	blood:	n/a	n/a
24	CREB1	chr6:75156690-75157148	GM12878	blood:	n/a	n/a
25	CTCF	chr6:75119254-75119472	Pancreas_OC	pancreas:	n/a	chr6:75119344-75119362
26	CTCF	chr6:74990096-74990307	MCF-7	breast:	n/a	n/a
27	CTCF	chr6:74990040-74990190	RPTEC	kidney:	n/a	n/a
28	CTCF	chr6:74990070-74990324	GM12878	blood:	n/a	n/a
29	CTCF	chr6:75053657-75053750	MCF-7	breast:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
30	CTCF	chr6:74989560-74989710	RPTEC	kidney:	n/a	chr6:74989638-74989647
31	CTCF	chr6:75119309-75119439	MCF-7	breast:	n/a	chr6:75119344-75119362
32	CTCF	chr6:75119280-75119430	HPF	lung:	n/a	chr6:75119344-75119362
33	CTCF	chr6:75019605-75019681	GM10248	blood:	n/a	n/a
34	CTCF	chr6:75053540-75053690	HVMF	connective:	n/a	n/a
35	CTCF	chr6:75053640-75053790	GM06990	blood:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
36	CTCF	chr6:75053665-75053770	Pancreas_OC	pancreas:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
37	CTCF	chr6:75053560-75053710	HAc	cerebellar:	n/a	n/a
38	CTCF	chr6:74990120-74990270	NB4	blood:	n/a	n/a
39	CTCF	chr6:75053686-75053729	Gliobla	brain:	n/a	chr6:75053717-75053726 chr6:75053719-75053729
40	CTCF	chr6:75020025-75020103	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:75053640-75053790	AG10803	skin:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
42	CTCF	chr6:75119259-75119457	LNCaP	prostate:	n/a	chr6:75119344-75119362
43	CTCF	chr6:75152617-75152699	GM13976	blood:	n/a	n/a
44	CTCF	chr6:75019980-75020130	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr6:75053526-75053818	HepG2	liver:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
46	CTCF	chr6:74990122-74990266	ProgFib	skin:	n/a	n/a
47	CTCF	chr6:74990060-74990210	HCFaa	heart:	n/a	n/a
48	CTCF	chr6:75020000-75020150	HCT-116	colon:	n/a	n/a
49	CTCF	chr6:75053589-75053876	MCF-7	breast:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
50	CTCF	chr6:74990100-74990250	HFF	foreskin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:74965323-74965373	AG04450	lung:	fetal
2	chr6:74978996-74979046	HUVEC	blood vessel:	n/a
3	chr6:75061364-75061414	HRE	kidney:	n/a
4	chr6:75079753-75079803	SK-N-SH_RA	brain:	n/a
5	chr6:74998385-74998435	HCT-116	colon:	n/a
6	chr6:75061364-75061414	GM19239	blood:	n/a
7	chr6:74978996-74979046	PANC-1	pancreas:	n/a
8	chr6:75079753-75079803	BJ	skin:	n/a
9	chr6:74987753-74987803	K562	blood:	n/a
10	chr6:74965323-74965373	PrEC	prostate:	n/a
11	chr6:74998385-74998435	Hela-S3	cervix:	n/a
12	chr6:74987753-74987803	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:74998385-74998435	AoSMC	blood vessel:	n/a
14	chr6:74987753-74987803	HCF	heart:	n/a
15	chr6:74998385-74998435	SKMC	muscle:	n/a
16	chr6:74978996-74979046	BE2_C	brain:	n/a
17	chr6:75079753-75079803	K562	blood:	n/a
18	chr6:74978996-74979046	A549	lung:	n/a
19	chr6:75079753-75079803	A549	lung:	n/a
20	chr6:74978996-74979046	NT2-D1	testis:	n/a
21	chr6:75061364-75061414	RPTEC	kidney:	n/a
22	chr6:74965323-74965373	HCPEpiC	choroid plexus:	n/a
23	chr6:74978996-74979046	HRE	kidney:	n/a
24	chr6:74998385-74998435	NHBE	bronchial:	n/a
25	chr6:74978996-74979046	HAEpiC	amniotic membrane:	n/a
26	chr6:75061364-75061414	HCPEpiC	choroid plexus:	n/a
27	chr6:74987753-74987803	HL-60	blood:	n/a
28	chr6:74998385-74998435	HAEpiC	amniotic membrane:	n/a
29	chr6:74998385-74998435	PrEC	prostate:	n/a
30	chr6:75079753-75079803	T-47D	breast:	n/a
31	chr6:75079753-75079803	NHBE	bronchial:	n/a
32	chr6:74978996-74979046	PFSK-1	brain:	n/a
33	chr6:75061364-75061414	SKMC	muscle:	n/a
34	chr6:75079753-75079803	ECC-1	luminal epithelium:	n/a
35	chr6:75079753-75079803	HRCEpiC	kidney:	n/a
36	chr6:74998385-74998435	PFSK-1	brain:	n/a
37	chr6:74987753-74987803	ovcar-3	ovarian:	n/a
38	chr6:74987753-74987803	SK-N-SH_RA	brain:	n/a
39	chr6:74987753-74987803	HRPEpiC	eye:	n/a
40	chr6:74978996-74979046	NB4	blood:	n/a
41	chr6:74965323-74965373	BJ	skin:	n/a
42	chr6:74987753-74987803	LNCaP	prostate:	n/a
43	chr6:74998385-74998435	SAEC	small airway:	n/a
44	chr6:74987753-74987803	PrEC	prostate:	n/a
45	chr6:75079753-75079803	AG10803	skin:	n/a
46	chr6:75061364-75061414	PrEC	prostate:	n/a
47	chr6:74998385-74998435	AG04449	skin:	fetal
48	chr6:75079753-75079803	AG04450	lung:	fetal
49	chr6:74978996-74979046	NHDF-neo	bronchial:	n/a
50	chr6:75079753-75079803	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:75012871..75015540-chr6:75027590..75030064,2	MCF-7	breast:
2	chr19:18479342..18480148-chr6:75021400..75022173,2	MCF-7	breast:
3	chr6:75117931..75120867-chr6:75914408..75916114,2	MCF-7	breast:
4	chr6:75118978..75119780-chr6:75475200..75475940,2	MCF-7	breast:
5	chr6:75012871..75015540-chr6:75027590..75030064,2	MCF-7	breast:
6	chr6:75026464..75029067-chr6:75031297..75033184,2	K562	blood:
7	chr6:75026464..75029067-chr6:75031297..75033184,2	K562	blood:
8	chr6:75053870..75055720-chr6:75913011..75915599,2	MCF-7	breast:
9	chr6:75007204..75009226-chr6:75014821..75017230,2	K562	blood:
10	chr6:75118557..75119496-chr6:75918100..75919176,3	MCF-7	breast:
11	chr6:75053590..75054206-chr6:75918614..75919395,2	MCF-7	breast:
12	chr6:75007204..75009226-chr6:75014821..75017230,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD109-8	chr6:75113511-75113565	ucscGeneNc_uc003phr_2
2	lnc-CD109-3	chr6:75056791-75056845	ENSG00000223786.1

Variant related genes	Relation type
ENSG00000217178	TF binding region
ENSG00000217178	CpG island
ENSG00000111799	chromatin interactions

Extended variants
information (count: 4273 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:4273 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55962148	chr6:74962021-74962022	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188007316	chr6:74962035-74962036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549295528	chr6:74962043-74962044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550261984	chr6:74962082-74962083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568654994	chr6:74962096-74962097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149932078	chr6:74962103-74962104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554345756	chr6:74962139-74962140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573065210	chr6:74962140-74962141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144265429	chr6:74962158-74962159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs117057752	chr6:74962162-74962163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577954129	chr6:74962165-74962166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181986557	chr6:74962192-74962193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186166985	chr6:74962214-74962215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369666459	chr6:74962221-74962222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148748698	chr6:74962227-74962228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190682296	chr6:74962228-74962229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373246266	chr6:74962251-74962252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142259518	chr6:74962278-74962279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546957714	chr6:74962299-74962300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115116399	chr6:74962307-74962308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377518929	chr6:74962357-74962358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113476888	chr6:74962404-74962405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114162887	chr6:74962421-74962422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs510526	chr6:74962435-74962436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373191187	chr6:74962480-74962481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs199865329	chr6:74962497-74962498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200679909	chr6:74962501-74962502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372587643	chr6:74962502-74962503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181513503	chr6:74962505-74962506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs202031501	chr6:74962523-74962524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201549614	chr6:74962563-74962564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548332853	chr6:74962581-74962582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2788987	chr6:74962590-74962591	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs2781175	chr6:74962615-74962616	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs113567503	chr6:74962741-74962742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558564732	chr6:74962760-74962761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566139886	chr6:74962762-74962763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577218118	chr6:74962771-74962772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144501401	chr6:74962778-74962779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557410116	chr6:74962802-74962803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186579356	chr6:74962804-74962805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543125215	chr6:74962807-74962808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146635788	chr6:74962812-74962813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573355317	chr6:74962825-74962826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540865741	chr6:74962913-74962914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141020804	chr6:74962918-74962919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532670021	chr6:74962924-74962925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2781174	chr6:74962935-74962936	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs11754988	chr6:74962938-74962939	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs529677317	chr6:74962975-74962976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Prostate cancer	16573809	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelodysplastic syndrome	18508791	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74959600-74963400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:74960400-74965600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:74961200-74962000	Enhancers	Colon Smooth Muscle	Colon
4	chr6:74961200-74962000	Enhancers	Stomach Smooth Muscle	stomach
5	chr6:74961400-74963200	Weak transcription	NHEK	skin
6	chr6:74961400-74966400	Weak transcription	NHLF	lung
7	chr6:74961600-74962200	Enhancers	Duodenum Smooth Muscle	Duodenum
8	chr6:74961600-74966600	Weak transcription	Adipose Nuclei	Adipose
9	chr6:74961800-74966600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr6:74963200-74964000	Enhancers	NHEK	skin
11	chr6:74963400-74964000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:74964800-74965000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:74965000-74967400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:74965600-74965800	Enhancers	Fetal Muscle Leg	muscle
15	chr6:74965600-74966800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:74965600-74967000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr6:74965600-74967000	Enhancers	Fetal Stomach	stomach
18	chr6:74965800-74966600	Weak transcription	Fetal Muscle Leg	muscle
19	chr6:74966200-74966800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr6:74966200-74967000	Enhancers	Fetal Intestine Small	intestine
21	chr6:74966400-74966800	Enhancers	NHDF-Ad	bronchial
22	chr6:74966400-74967000	Enhancers	Fetal Intestine Large	intestine
23	chr6:74966600-74966800	Enhancers	Fetal Muscle Leg	muscle
24	chr6:74966600-74967000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr6:74966600-74967000	Enhancers	Adipose Nuclei	Adipose
26	chr6:74966600-74967000	Enhancers	Fetal Lung	lung
27	chr6:74966600-74967000	Enhancers	Left Ventricle	heart
28	chr6:74966800-74969000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:74967000-74967200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr6:74967000-74968400	Weak transcription	Fetal Stomach	stomach
31	chr6:74967000-74969400	Weak transcription	Adipose Nuclei	Adipose
32	chr6:74968400-74968600	Enhancers	Fetal Stomach	stomach
33	chr6:74968400-74969200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr6:74969000-74970200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:74969400-74969800	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr6:74969400-74970000	Enhancers	Adipose Nuclei	Adipose
37	chr6:74969400-74970000	Enhancers	Ovary	ovary
38	chr6:74973200-74974000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr6:74974000-74975200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr6:74975400-74975600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr6:74976600-74976800	Enhancers	Fetal Muscle Leg	muscle
42	chr6:74976800-74979000	Weak transcription	Fetal Muscle Leg	muscle
43	chr6:74978200-74979400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr6:74979000-74979400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr6:74979000-74979400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr6:74979000-74979400	Enhancers	Fetal Muscle Leg	muscle
47	chr6:74979000-74979400	Enhancers	NHDF-Ad	bronchial
48	chr6:74979000-74979600	Enhancers	Fetal Stomach	stomach
49	chr6:74979200-74979400	Bivalent Enhancer	HSMMtube	muscle
50	chr6:74979400-74979600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links