Variant report

Variant	nsv970370
Chromosome Location	chr6:4605843-4619763
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:183)
CpG islands
(count:244)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:183 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:4612951-4613063	K562	blood:	n/a	n/a
2	BCL11A	chr6:4607739-4608000	GM12878	blood:	n/a	n/a
3	BHLHE40	chr6:4619670-4619703	K562	blood:	n/a	n/a
4	BHLHE40	chr6:4612860-4613059	K562	blood:	n/a	n/a
5	CCNT2	chr6:4612812-4613192	K562	blood:	n/a	n/a
6	CEBPB	chr6:4607574-4608050	ECC-1	luminal epithelium:	n/a	n/a
7	CEBPB	chr6:4612912-4613230	IMR90	lung:	n/a	n/a
8	CEBPB	chr6:4607527-4608093	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr6:4612796-4613107	K562	blood:	n/a	n/a
10	CEBPB	chr6:4612844-4613201	K562	blood:	n/a	n/a
11	CEBPB	chr6:4607662-4608058	MCF-7	breast:	n/a	n/a
12	CEBPB	chr6:4616293-4616543	IMR90	lung:	n/a	n/a
13	CHD2	chr6:4611898-4612157	GM12878	blood:	n/a	n/a
14	CTCF	chr6:4606260-4606410	K562	blood:	n/a	n/a
15	CTCF	chr6:4616200-4616350	AoAF	blood vessel:	n/a	chr6:4616274-4616287
16	CTCF	chr6:4618980-4619130	GM12865	blood:	n/a	n/a
17	CTCF	chr6:4607420-4607570	HMEC	breast:	n/a	n/a
18	CTCF	chr6:4606540-4606690	K562	blood:	n/a	n/a
19	CTCF	chr6:4606600-4606750	GM12871	blood:	n/a	n/a
20	CTCF	chr6:4607380-4607530	GM12875	blood:	n/a	n/a
21	CTCF	chr6:4610360-4610510	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr6:4616140-4616290	HPAF	blood vessel:	n/a	chr6:4616274-4616287
23	E2F4	chr6:4607549-4607916	MCF10A-Er-Src	breast:	n/a	n/a
24	EBF1	chr6:4611937-4612174	GM12878	blood:	n/a	chr6:4612067-4612078
25	EBF1	chr6:4610651-4610749	GM12878	blood:	n/a	n/a
26	EBF1	chr6:4611869-4612184	GM12878	blood:	n/a	chr6:4612067-4612078
27	EBF1	chr6:4611896-4612249	GM12878	blood:	n/a	chr6:4612067-4612078
28	EP300	chr6:4607605-4607997	SK-N-SH_RA	brain:	n/a	chr6:4607790-4607799
29	EP300	chr6:4607560-4608018	T-47D	breast:	n/a	chr6:4607790-4607799
30	EP300	chr6:4607239-4608171	ECC-1	luminal epithelium:	n/a	chr6:4607790-4607799
31	EP300	chr6:4607401-4608063	T-47D	breast:	n/a	chr6:4607790-4607799
32	EP300	chr6:4610527-4610847	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr6:4607031-4608244	ECC-1	luminal epithelium:	n/a	chr6:4607790-4607799 chr6:4607179-4607193
34	EP300	chr6:4607528-4608046	MCF-7	breast:	n/a	chr6:4607790-4607799
35	EP300	chr6:4610472-4610832	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr6:4612855-4613097	K562	blood:	n/a	n/a
37	EP300	chr6:4607401-4608042	SK-N-SH_RA	brain:	n/a	chr6:4607790-4607799
38	ESR1	chr6:4607538-4608012	T-47D	breast:	n/a	n/a
39	ESR1	chr6:4607546-4608034	T-47D	breast:	n/a	n/a
40	ESR1	chr6:4607568-4607965	T-47D	breast:	n/a	n/a
41	ESR1	chr6:4607565-4608048	ECC-1	luminal epithelium:	n/a	n/a
42	ESR1	chr6:4607249-4608086	ECC-1	luminal epithelium:	n/a	n/a
43	ESR1	chr6:4607342-4608159	ECC-1	luminal epithelium:	n/a	n/a
44	ESR1	chr6:4607633-4607979	T-47D	breast:	n/a	n/a
45	ESR1	chr6:4607424-4608147	ECC-1	luminal epithelium:	n/a	n/a
46	FOS	chr6:4607554-4608005	MCF10A-Er-Src	breast:	n/a	chr6:4607669-4607676 chr6:4607792-4607799 chr6:4607659-4607667 chr6:4607789-4607800 chr6:4607790-4607799
47	FOS	chr6:4607650-4607966	Hela-S3	cervix:	n/a	chr6:4607669-4607676 chr6:4607792-4607799 chr6:4607659-4607667 chr6:4607789-4607800 chr6:4607790-4607799
48	FOS	chr6:4607256-4607354	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr6:4607575-4607997	MCF10A-Er-Src	breast:	n/a	chr6:4607669-4607676 chr6:4607792-4607799 chr6:4607659-4607667 chr6:4607789-4607800 chr6:4607790-4607799
50	FOS	chr6:4607287-4607359	MCF10A-Er-Src	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:4610716-4610766	GM12891	blood:	n/a
2	chr6:4607680-4607730	GM12891	blood:	n/a
3	chr6:4610716-4610766	AG04449	skin:	fetal
4	chr6:4610716-4610766	ECC-1	luminal epithelium:	n/a
5	chr6:4610716-4610766	PFSK-1	brain:	n/a
6	chr6:4607680-4607730	U87	brain:	n/a
7	chr6:4610716-4610766	HEEpiC	esophagus:	n/a
8	chr6:4610575-4610625	SK-N-SH_RA	brain:	n/a
9	chr6:4610575-4610625	HL-60	blood:	n/a
10	chr6:4607680-4607730	GM06990	blood:	n/a
11	chr6:4610716-4610766	CMK	blood:	n/a
12	chr6:4610575-4610625	ovcar-3	ovarian:	n/a
13	chr6:4610716-4610766	T-47D	breast:	n/a
14	chr6:4610716-4610766	Jurkat	blood:	n/a
15	chr6:4607680-4607730	ProgFib	skin:	n/a
16	chr6:4610575-4610625	PrEC	prostate:	n/a
17	chr6:4610716-4610766	GM12892	blood:	n/a
18	chr6:4610575-4610625	NHDF-neo	bronchial:	n/a
19	chr6:4610716-4610766	ovcar-3	ovarian:	n/a
20	chr6:4612064-4612114	Jurkat	blood:	n/a
21	chr6:4610575-4610625	MCF-7	breast:	n/a
22	chr6:4610575-4610625	MCF10A-Er-Src	breast:	n/a
23	chr6:4607680-4607730	HCPEpiC	choroid plexus:	n/a
24	chr6:4610575-4610625	GM12878	blood:	n/a
25	chr6:4610575-4610625	NT2-D1	testis:	n/a
26	chr6:4610716-4610766	HNPCEpiC	eye:	n/a
27	chr6:4610716-4610766	AG09319	gingival:	n/a
28	chr6:4610575-4610625	ProgFib	skin:	n/a
29	chr6:4607680-4607730	AoSMC	blood vessel:	n/a
30	chr6:4612064-4612114	MCF-7	breast:	n/a
31	chr6:4610575-4610625	ECC-1	luminal epithelium:	n/a
32	chr6:4610575-4610625	LNCaP	prostate:	n/a
33	chr6:4610716-4610766	MCF10A-Er-Src	breast:	n/a
34	chr6:4607680-4607730	HUVEC	blood vessel:	n/a
35	chr6:4607680-4607730	HRE	kidney:	n/a
36	chr6:4610575-4610625	HCM	heart:	n/a
37	chr6:4610716-4610766	A549	lung:	n/a
38	chr6:4607680-4607730	SKMC	muscle:	n/a
39	chr6:4610716-4610766	ProgFib	skin:	n/a
40	chr6:4610716-4610766	PANC-1	pancreas:	n/a
41	chr6:4610575-4610625	HRPEpiC	eye:	n/a
42	chr6:4612064-4612114	AG04450	lung:	fetal
43	chr6:4610716-4610766	Caco-2	colon:	n/a
44	chr6:4607680-4607730	HepG2	liver:	n/a
45	chr6:4607680-4607730	HMEC	breast:	n/a
46	chr6:4610575-4610625	AG04450	lung:	fetal
47	chr6:4607680-4607730	AG04450	lung:	fetal
48	chr6:4610716-4610766	NT2-D1	testis:	n/a
49	chr6:4607680-4607730	HEK293	kidney:	embryo
50	chr6:4612064-4612114	K562	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:4609256..4612508-chr6:4614034..4616803,3	MCF-7	breast:
2	chr6:4585158..4587342-chr6:4603749..4606503,2	MCF-7	breast:
3	chr6:4601505..4603151-chr6:4605939..4607714,2	MCF-7	breast:
4	chr6:4608105..4609645-chr6:4609883..4611653,2	MCF-7	breast:
5	chr6:4606412..4609387-chr6:4772936..4775041,2	MCF-7	breast:
6	chr6:4615595..4617785-chr6:4618078..4620387,2	MCF-7	breast:
7	chr6:4615595..4617785-chr6:4618078..4620387,2	MCF-7	breast:
8	chr6:4606187..4608803-chr6:4609320..4611011,2	K562	blood:
9	chr6:4617288..4619775-chr6:4621638..4623955,2	MCF-7	breast:
10	chr6:4612784..4615620-chr6:4617174..4619845,3	MCF-7	breast:
11	chr6:4612784..4615620-chr6:4617174..4619845,3	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDYL-1	chr6:4611212-4612152	XLOC_005142
2	lnc-CDYL-1	chr6:4610846-4611046	XLOC_005142

No data

Variant related genes	Relation type
ENSG00000205444	TF binding region
ENSG00000260673	TF binding region
ENSG00000205444	CpG island
ENSG00000260673	CpG island
ENSG00000260673	chromatin interactions
ENSG00000153046	chromatin interactions
ENSG00000205444	chromatin interactions

Extended variants
information (count: 584 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186840143	chr6:4605869-4605870	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542480482	chr6:4605915-4605916	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571937086	chr6:4605949-4605950	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs35426498	chr6:4605965-4605966	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs192605226	chr6:4606033-4606034	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs559367508	chr6:4606048-4606049	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs115593149	chr6:4606053-4606054	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs545001033	chr6:4606065-4606066	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs564923667	chr6:4606068-4606069	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs530526756	chr6:4606088-4606089	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs550448401	chr6:4606132-4606133	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs386696422	chr6:4606154-4606155	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs11964427	chr6:4606156-4606157	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs142902563	chr6:4606180-4606181	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs184775904	chr6:4606197-4606198	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs372754397	chr6:4606210-4606211	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs143212674	chr6:4606217-4606218	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs57689506	chr6:4606219-4606220	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs376001795	chr6:4606260-4606261	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs188092282	chr6:4606273-4606274	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs551352532	chr6:4606373-4606374	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs370092104	chr6:4606381-4606382	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs537050933	chr6:4606384-4606385	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs557194694	chr6:4606395-4606396	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs546171120	chr6:4606417-4606418	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs545833155	chr6:4606436-4606437	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs548282209	chr6:4606437-4606438	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs151090833	chr6:4606467-4606468	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs78395407	chr6:4606494-4606495	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs572962432	chr6:4606495-4606496	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs141069508	chr6:4606507-4606508	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs558697735	chr6:4606521-4606522	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs562913747	chr6:4606524-4606525	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs201460594	chr6:4606532-4606533	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs531835129	chr6:4606591-4606592	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs369613537	chr6:4606598-4606599	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs575279854	chr6:4606605-4606606	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs543888875	chr6:4606657-4606658	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs193000359	chr6:4606660-4606661	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs373124501	chr6:4606662-4606663	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs185204458	chr6:4606689-4606690	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs548749366	chr6:4606716-4606717	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs543197163	chr6:4606727-4606728	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs189469745	chr6:4606747-4606748	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs149794313	chr6:4606785-4606786	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs551420272	chr6:4606812-4606813	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs181941286	chr6:4606829-4606830	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs114767436	chr6:4606866-4606867	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs113089404	chr6:4606956-4606957	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs563230921	chr6:4606992-4606993	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4600000-4606800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr6:4601000-4607000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr6:4601200-4606400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:4601200-4606400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr6:4601200-4606400	Weak transcription	Right Ventricle	heart
6	chr6:4601400-4607000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:4601600-4606000	Weak transcription	Fetal Muscle Leg	muscle
8	chr6:4601600-4606800	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr6:4601800-4607000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr6:4602600-4606400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:4603400-4608800	Weak transcription	Spleen	Spleen
12	chr6:4603600-4606400	Weak transcription	Adipose Nuclei	Adipose
13	chr6:4603600-4606800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr6:4603600-4607200	Weak transcription	Esophagus	oesophagus
15	chr6:4603800-4606400	Weak transcription	Lung	lung
16	chr6:4604000-4606800	Weak transcription	HSMMtube	muscle
17	chr6:4604000-4607200	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr6:4604000-4607200	Weak transcription	NHLF	lung
19	chr6:4604400-4606200	Weak transcription	HMEC	breast
20	chr6:4604400-4606400	Weak transcription	Placenta	Placenta
21	chr6:4604400-4606600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr6:4604400-4606600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr6:4604400-4606600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr6:4604400-4606600	Weak transcription	Osteobl	bone
25	chr6:4604400-4606800	Weak transcription	HUVEC	blood vessel
26	chr6:4604400-4606800	Weak transcription	NH-A	brain
27	chr6:4604400-4607000	Weak transcription	NHDF-Ad	bronchial
28	chr6:4604400-4607200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:4604400-4607200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr6:4604400-4607800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr6:4604400-4610200	Weak transcription	Fetal Heart	heart
32	chr6:4604600-4606400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:4604600-4606400	Weak transcription	HSMM	muscle
34	chr6:4605400-4607000	Weak transcription	Right Atrium	heart
35	chr6:4605400-4607600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr6:4605800-4606800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:4606000-4607200	Enhancers	Fetal Muscle Trunk	muscle
38	chr6:4606000-4616800	Enhancers	Fetal Muscle Leg	muscle
39	chr6:4606200-4607000	Enhancers	HMEC	breast
40	chr6:4606400-4606600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr6:4606400-4607000	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr6:4606400-4607000	Enhancers	Brain Angular Gyrus	brain
43	chr6:4606400-4607000	Enhancers	Brain Hippocampus Middle	brain
44	chr6:4606400-4607000	Enhancers	Brain Substantia Nigra	brain
45	chr6:4606400-4607000	Enhancers	Stomach Smooth Muscle	stomach
46	chr6:4606400-4607000	Enhancers	HSMM	muscle
47	chr6:4606400-4607200	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr6:4606400-4607600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr6:4606400-4607600	Enhancers	Lung	lung
50	chr6:4606400-4607600	Enhancers	Right Ventricle	heart

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