Variant report

Variant	nsv428778
Chromosome Location	chr4:186933032-187056322
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	chr4:186942758-186943110	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:186989219-186989538	HepG2	liver:	n/a	n/a
3	ATF1	chr4:187027151-187027480	K562	blood:	n/a	n/a
4	ATF2	chr4:187055315-187055866	GM12878	blood:	n/a	n/a
5	ATF2	chr4:187027166-187027483	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:186979842-186980247	GM12878	blood:	n/a	n/a
7	BACH1	chr4:187025719-187026243	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:187026701-187026862	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr4:186979789-186980186	GM12878	blood:	n/a	n/a
10	BATF	chr4:187055418-187055866	GM12878	blood:	n/a	n/a
11	BATF	chr4:186954961-186955292	GM12878	blood:	n/a	n/a
12	BATF	chr4:187055371-187055785	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:186979842-186980224	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:187055420-187055843	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:186979854-186980169	GM12878	blood:	n/a	n/a
16	BCL3	chr4:186979865-186980155	GM12878	blood:	n/a	n/a
17	BCL3	chr4:187055433-187055716	GM12878	blood:	n/a	n/a
18	BCL3	chr4:186979857-186980236	GM12878	blood:	n/a	n/a
19	BCLAF1	chr4:187055428-187055813	GM12878	blood:	n/a	n/a
20	BCLAF1	chr4:187055345-187055835	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:187055496-187055825	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:186959317-186959495	K562	blood:	n/a	n/a
23	BHLHE40	chr4:187039012-187039026	K562	blood:	n/a	n/a
24	CBX3	chr4:186989030-186989622	HCT-116	colon:	n/a	chr4:186989176-186989187
25	CEBPB	chr4:186945933-186946103	K562	blood:	n/a	n/a
26	CEBPB	chr4:186982076-186982118	HepG2	liver:	n/a	chr4:186982090-186982101
27	CEBPB	chr4:187037874-187038237	H1-hESC	embryonic stem cell:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
28	CEBPB	chr4:186945853-186946131	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr4:187037849-187038207	ECC-1	luminal epithelium:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
30	CEBPB	chr4:186959423-186959701	K562	blood:	n/a	n/a
31	CEBPB	chr4:187037900-187038225	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
32	CEBPB	chr4:187037868-187038236	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
33	CEBPB	chr4:186953062-186953236	Hela-S3	cervix:	n/a	chr4:186953179-186953190 chr4:186953180-186953191 chr4:186953179-186953192
34	CEBPB	chr4:186959441-186959724	A549	lung:	n/a	n/a
35	CEBPB	chr4:187037872-187038236	IMR90	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
36	CEBPB	chr4:186961659-186961834	A549	lung:	n/a	n/a
37	CEBPB	chr4:186990084-186990532	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr4:186959311-186959753	Hela-S3	cervix:	n/a	chr4:186959418-186959429
39	CEBPB	chr4:187037867-187038233	HepG2	liver:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
40	CEBPB	chr4:186945896-186946153	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:187037859-187038158	MCF-7	breast:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
42	CEBPB	chr4:187037881-187038220	Hela-S3	cervix:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
43	CEBPB	chr4:186945861-186946131	MCF-7	breast:	n/a	n/a
44	CEBPB	chr4:187037845-187038266	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
45	CEBPB	chr4:186961634-186961797	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:186949884-186950178	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr4:187037865-187038243	K562	blood:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
48	CEBPB	chr4:186945975-186946048	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr4:187037847-187038225	ECC-1	luminal epithelium:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
50	CEBPB	chr4:186953031-186953345	HepG2	liver:	n/a	chr4:186953179-186953190 chr4:186953180-186953191 chr4:186953179-186953192

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:186945339-186945389	Jurkat	blood:	n/a
2	chr4:186944988-186945038	HRPEpiC	eye:	n/a
3	chr4:187000846-187000896	Jurkat	blood:	n/a
4	chr4:187013536-187013586	HCM	heart:	n/a
5	chr4:186960991-186961041	RPTEC	kidney:	n/a
6	chr4:187037318-187037368	HL-60	blood:	n/a
7	chr4:186945339-186945389	Jurkat	blood:	n/a
8	chr4:186944988-186945038	HRPEpiC	eye:	n/a
9	chr4:187000846-187000896	Jurkat	blood:	n/a
10	chr4:187013536-187013586	HCM	heart:	n/a
11	chr4:186960991-186961041	RPTEC	kidney:	n/a
12	chr4:187037318-187037368	HL-60	blood:	n/a
13	chr4:186951273-186951323	HL-60	blood:	n/a
14	chr4:187025897-187025947	PANC-1	pancreas:	n/a
15	chr4:186990006-186990056	BJ	skin:	n/a
16	chr4:187026710-187026760	MCF10A-Er-Src	breast:	n/a
17	chr4:187026710-187026760	ProgFib	skin:	n/a
18	chr4:186990425-186990475	Hela-S3	cervix:	n/a
19	chr4:186990324-186990374	HNPCEpiC	eye:	n/a
20	chr4:187003000-187003050	SKMC	muscle:	n/a
21	chr4:187013645-187013695	SKMC	muscle:	n/a
22	chr4:186945339-186945389	ovcar-3	ovarian:	n/a
23	chr4:186945339-186945389	SAEC	small airway:	n/a
24	chr4:187025654-187025704	Caco-2	colon:	n/a
25	chr4:186990006-186990056	MCF-7	breast:	n/a
26	chr4:186990315-186990365	MCF-7	breast:	n/a
27	chr4:186944909-186944959	T-47D	breast:	n/a
28	chr4:186945215-186945265	CMK	blood:	n/a
29	chr4:187037256-187037306	HUVEC	blood vessel:	n/a
30	chr4:187013536-187013586	NHDF-neo	bronchial:	n/a
31	chr4:187013536-187013586	T-47D	breast:	n/a
32	chr4:187026872-187026922	BJ	skin:	n/a
33	chr4:187026872-187026922	HCPEpiC	choroid plexus:	n/a
34	chr4:187026225-187026275	H1-hESC	embryonic stem cell:	embryo
35	chr4:186945339-186945389	AG09309	skin:	n/a
36	chr4:187053574-187053624	MCF10A-Er-Src	breast:	n/a
37	chr4:187026225-187026275	AG04450	lung:	fetal
38	chr4:186945215-186945265	SAEC	small airway:	n/a
39	chr4:186951273-186951323	SK-N-SH	brain:	n/a
40	chr4:186945339-186945389	T-47D	breast:	n/a
41	chr4:186990006-186990056	GM12891	blood:	n/a
42	chr4:187025420-187025470	AG09319	gingival:	n/a
43	chr4:187003000-187003050	HUVEC	blood vessel:	n/a
44	chr4:187026278-187026328	HEEpiC	esophagus:	n/a
45	chr4:187037318-187037368	Jurkat	blood:	n/a
46	chr4:186945215-186945265	NH-A	brain:	n/a
47	chr4:187026872-187026922	GM06990	blood:	n/a
48	chr4:187026278-187026328	HIPEpiC	eye:	n/a
49	chr4:186945339-186945389	HNPCEpiC	eye:	n/a
50	chr4:186944909-186944959	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:186933593..186936469-chr4:186945344..186948028,2	K562	blood:
2	chr4:186981542..186984257-chr4:186986669..186988190,2	MCF-7	breast:
3	chr4:187002937..187005829-chr4:187012756..187015507,2	MCF-7	breast:
4	chr4:186985477..186986987-chr4:187047828..187050010,2	K562	blood:
5	chr4:187009172..187011759-chr4:187017494..187019918,3	K562	blood:
6	chr4:186985477..186986987-chr4:187047828..187050010,2	K562	blood:
7	chr4:186561919..186562574-chr4:186942657..186943394,3	MCF-7	breast:
8	chr4:186988895..186989419-chr4:187058283..187058978,2	K562	blood:
9	chr4:187053833..187057505-chr4:187060435..187064133,3	K562	blood:
10	chr4:186561682..186562601-chr4:186936140..186936998,3	MCF-7	breast:
11	chr4:187036166..187038039-chr4:187110587..187113537,2	K562	blood:
12	chr4:187053677..187057505-chr4:187060435..187064236,4	K562	blood:
13	chr4:187000465..187002106-chr4:187010501..187012706,2	MCF-7	breast:
14	chr4:186561687..186562665-chr4:186959039..186959962,3	MCF-7	breast:
15	chr4:187002937..187005829-chr4:187012756..187015507,2	MCF-7	breast:
16	chr4:186988828..186989568-chr4:187053779..187054412,2	MCF-7	breast:
17	chr4:186953201..186953720-chr4:187058277..187058867,2	MCF-7	breast:
18	chr4:187000465..187002106-chr4:187010501..187012706,2	MCF-7	breast:
19	chr4:186988972..186989928-chr4:187122701..187123491,2	MCF-7	breast:
20	chr4:187009172..187011759-chr4:187017494..187019918,3	K562	blood:
21	chr4:187023730..187026664-chr4:187030524..187032198,2	MCF-7	breast:
22	chr16:17073810..17074454-chr4:186958456..186959434,2	MCF-7	breast:
23	chr4:186543758..186545756-chr4:186936731..186939343,2	K562	blood:
24	chr4:186988828..186989568-chr4:187053779..187054412,2	MCF-7	breast:
25	chr4:187021448..187022968-chr6:31674535..31677393,2	K562	blood:
26	chr4:186981542..186984257-chr4:186986669..186988190,2	MCF-7	breast:
27	chr4:186988859..186989716-chr4:187058329..187059203,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TLR3-1	chr4:186939607-186940103	XLOC_003820
2	lnc-TLR3-1	chr4:186936734-186936900	XLOC_003820
3	lnc-SORBS2-2	chr4:186940952-186941235	XLOC_004212
4	lnc-SORBS2-2	chr4:186937392-186938595	XLOC_004212
5	lnc-TLR3-1	chr4:186938433-186938541	XLOC_003820

Variant related genes	Relation type
ENSG00000253013	TF binding region
FAM149A	TF binding region
RNU4-64P	TF binding region
TLR3	TF binding region
ENSG00000253013	CpG island
FAM149A	CpG island
RNU4-64P	CpG island
TLR3	CpG island
ENSG00000109794	chromatin interactions
ENSG00000250641	chromatin interactions
ENSG00000145476	chromatin interactions
ENSG00000204424	chromatin interactions
ENSG00000222727	chromatin interactions
ENSG00000269302	chromatin interactions

Extended variants
information (count: 5070 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:5070 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548398429	chr4:186933035-186933036	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs568427842	chr4:186933037-186933038	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs534205346	chr4:186933116-186933117	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs553279524	chr4:186933141-186933142	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs28561654	chr4:186933150-186933151	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs140812767	chr4:186933151-186933152	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs187057713	chr4:186933152-186933153	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs113476209	chr4:186933153-186933154	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs544253470	chr4:186933162-186933163	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs559693703	chr4:186933179-186933180	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs560835941	chr4:186933204-186933205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191801837	chr4:186933221-186933222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537174713	chr4:186933244-186933245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560398312	chr4:186933250-186933251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184092200	chr4:186933263-186933264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552496544	chr4:186933292-186933293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563053887	chr4:186933339-186933340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569081509	chr4:186933369-186933370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531823406	chr4:186933376-186933377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201116375	chr4:186933390-186933391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113285728	chr4:186933391-186933392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548633513	chr4:186933392-186933393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187574071	chr4:186933426-186933427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs527668125	chr4:186933481-186933482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547850094	chr4:186933493-186933494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145538983	chr4:186933511-186933512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538879135	chr4:186933517-186933518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558585097	chr4:186933525-186933526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569000901	chr4:186933535-186933536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537668802	chr4:186933542-186933543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554222742	chr4:186933546-186933547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148848821	chr4:186933572-186933573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143359893	chr4:186933611-186933612	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553401239	chr4:186933613-186933614	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs77008515	chr4:186933636-186933637	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs368696953	chr4:186933650-186933651	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs190046153	chr4:186933683-186933684	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531910140	chr4:186933741-186933742	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574815759	chr4:186933772-186933773	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs182601502	chr4:186933774-186933775	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs113989070	chr4:186933822-186933823	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs527834262	chr4:186933852-186933853	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs79183390	chr4:186933855-186933856	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs554096719	chr4:186933894-186933895	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs563473392	chr4:186933909-186933910	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs533186703	chr4:186933916-186933917	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs577226027	chr4:186933924-186933925	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs386683452	chr4:186933934-186933935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs1869619	chr4:186933936-186933937	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs187292247	chr4:186933958-186933959	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
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
Acute lymphoblastic leukemia	20067559	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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17086460	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1850 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:186919800-186936400	Weak transcription	Right Atrium	heart
2	chr4:186928600-186934200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr4:186929600-186937400	Weak transcription	Spleen	Spleen
4	chr4:186933000-186933200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:186933000-186933200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:186933000-186933600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr4:186933200-186934000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:186933200-186934200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:186933200-186935000	Enhancers	Fetal Heart	heart
10	chr4:186933400-186934200	Enhancers	Right Ventricle	heart
11	chr4:186933600-186934800	Enhancers	Left Ventricle	heart
12	chr4:186933800-186935400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:186933800-186935800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr4:186934000-186934800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr4:186934000-186935400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr4:186934200-186934800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:186934200-186935000	Enhancers	H9 Cell Line	embryonic stem cell
18	chr4:186934200-186935000	Enhancers	Fetal Lung	lung
19	chr4:186934200-186935400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr4:186934200-186935800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr4:186934200-186936400	Weak transcription	Right Ventricle	heart
22	chr4:186934200-186936600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr4:186934400-186934600	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr4:186934600-186934800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr4:186934600-186935000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr4:186934600-186935000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr4:186934600-186935400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr4:186934800-186935000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr4:186934800-186935200	Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr4:186934800-186936400	Weak transcription	Left Ventricle	heart
31	chr4:186934800-186946400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:186934800-186950400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr4:186935000-186936400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr4:186935000-186936400	Weak transcription	Fetal Heart	heart
35	chr4:186935000-186939000	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr4:186935000-186942000	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr4:186935200-186935400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr4:186935400-186936400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr4:186935400-186936400	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr4:186935400-186936600	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr4:186935400-186938600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr4:186935400-186939000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:186935800-186936200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr4:186936200-186936800	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:186936400-186936600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr4:186936400-186936600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr4:186936400-186936600	Enhancers	Right Atrium	heart
48	chr4:186936400-186936600	Flanking Active TSS	HSMMtube	muscle
49	chr4:186936400-186936800	Enhancers	Placenta	Placenta
50	chr4:186936400-186936800	Active TSS	Left Ventricle	heart

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