Variant report

Variant	nsv879221
Chromosome Location	chr4:68915798-69033099
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:403)
CpG islands
(count:488)
Chromatin interactive
region (count:27)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:68995505-68995878	K562	blood:	n/a	n/a
2	ATF1	chr4:68995507-68995848	K562	blood:	n/a	n/a
3	ATF1	chr4:69014644-69014829	K562	blood:	n/a	n/a
4	ATF1	chr4:69018227-69018433	K562	blood:	n/a	n/a
5	ATF3	chr4:68995610-68995980	K562	blood:	n/a	n/a
6	BACH1	chr4:68990022-68990381	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr4:68995560-68995938	K562	blood:	n/a	n/a
8	CBX3	chr4:69012748-69013185	K562	blood:	n/a	n/a
9	CBX3	chr4:69012824-69013135	K562	blood:	n/a	n/a
10	CBX3	chr4:68995389-68995866	K562	blood:	n/a	n/a
11	CBX3	chr4:68995373-68995867	HCT-116	colon:	n/a	n/a
12	CCNT2	chr4:68995497-68995943	K562	blood:	n/a	n/a
13	CEBPB	chr4:68987327-68987697	K562	blood:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
14	CEBPB	chr4:68926863-68927089	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:68939433-68939695	HepG2	liver:	n/a	chr4:68939507-68939518
16	CEBPB	chr4:68995579-68995924	K562	blood:	n/a	n/a
17	CEBPB	chr4:68926854-68927085	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:68987328-68987795	H1-hESC	embryonic stem cell:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
19	CEBPB	chr4:68995621-68995932	K562	blood:	n/a	n/a
20	CEBPB	chr4:68940212-68940475	HepG2	liver:	n/a	chr4:68940343-68940354
21	CEBPB	chr4:68940238-68940438	A549	lung:	n/a	chr4:68940343-68940354
22	CEBPB	chr4:69015854-69016082	HepG2	liver:	n/a	chr4:69015942-69015953
23	CEBPB	chr4:69014522-69014797	K562	blood:	n/a	n/a
24	CEBPB	chr4:69015863-69016001	K562	blood:	n/a	chr4:69015942-69015953
25	CEBPB	chr4:68995482-68995898	MCF-7	breast:	n/a	n/a
26	CEBPB	chr4:68939459-68939688	IMR90	lung:	n/a	chr4:68939507-68939518
27	CEBPB	chr4:68940147-68940530	Hela-S3	cervix:	n/a	chr4:68940343-68940354
28	CEBPB	chr4:69014530-69014780	K562	blood:	n/a	n/a
29	CREB1	chr4:68989221-68989671	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr4:68989350-68989616	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:68942020-68942170	K562	blood:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
32	CTCF	chr4:68945747-68945824	NHEK	skin:	n/a	chr4:68945782-68945798 chr4:68945783-68945804 chr4:68945781-68945799
33	CTCF	chr4:68945663-68945828	K562	blood:	n/a	chr4:68945782-68945798 chr4:68945783-68945804 chr4:68945781-68945799
34	CTCF	chr4:68942060-68942210	SAEC	small airway:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
35	CTCF	chr4:68942047-68942200	MCF-7	breast:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
36	CTCF	chr4:68942051-68942156	LNCaP	prostate:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
37	CTCF	chr4:68942085-68942141	LNCaP	prostate:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
38	CTCF	chr4:68942000-68942150	WERI-Rb-1	eye:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
39	CTCF	chr4:68942034-68942176	SK-N-SH_RA	brain:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
40	CTCF	chr4:68942060-68942210	HCT-116	colon:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
41	CTCF	chr4:68942080-68942230	NHEK	skin:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
42	CTCF	chr4:68933667-68933717	GM12878	blood:	n/a	n/a
43	CTCF	chr4:68942020-68942170	GM12872	blood:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
44	CTCF	chr4:68945711-68945854	MCF-7	breast:	n/a	chr4:68945782-68945798 chr4:68945783-68945804 chr4:68945781-68945799
45	CTCF	chr4:68945563-68945950	MCF-7	breast:	n/a	chr4:68945782-68945798 chr4:68945783-68945804 chr4:68945781-68945799
46	CTCF	chr4:68933659-68933725	NHEK	skin:	n/a	n/a
47	CTCF	chr4:68945840-68945990	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr4:68945720-68945870	HMEC	breast:	n/a	chr4:68945782-68945798 chr4:68945783-68945804 chr4:68945781-68945799
49	CTCF	chr4:68942054-68942203	GM12878	blood:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
50	CTCF	chr4:68933540-68933690	GM12878	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68995759-68995809	GM19239	blood:	n/a
2	chr4:68995759-68995809	AoSMC	blood vessel:	n/a
3	chr4:68995759-68995809	BJ	skin:	n/a
4	chr4:68928981-68929031	NH-A	brain:	n/a
5	chr4:68928981-68929031	GM12891	blood:	n/a
6	chr4:68929005-68929055	MCF10A-Er-Src	breast:	n/a
7	chr4:68995759-68995809	Hepatocyte	liver:	n/a
8	chr4:68928981-68929031	NHBE	bronchial:	n/a
9	chr4:68929005-68929055	HepG2	liver:	n/a
10	chr4:68929020-68929070	NT2-D1	testis:	n/a
11	chr4:68929413-68929463	HUVEC	blood vessel:	n/a
12	chr4:68928981-68929031	MCF-7	breast:	n/a
13	chr4:68928981-68929031	NHDF-neo	bronchial:	n/a
14	chr4:68929020-68929070	AG04449	skin:	fetal
15	chr4:68930433-68930483	HCT-116	colon:	n/a
16	chr4:68929005-68929055	SK-N-SH	brain:	n/a
17	chr4:68919575-68919625	HIPEpiC	eye:	n/a
18	chr4:68995995-68996045	PFSK-1	brain:	n/a
19	chr4:68929005-68929055	U87	brain:	n/a
20	chr4:68929413-68929463	ProgFib	skin:	n/a
21	chr4:68930433-68930483	HNPCEpiC	eye:	n/a
22	chr4:68929413-68929463	PrEC	prostate:	n/a
23	chr4:68930433-68930483	HRE	kidney:	n/a
24	chr4:68919575-68919625	AG04450	lung:	fetal
25	chr4:68930433-68930483	MCF-7	breast:	n/a
26	chr4:68995759-68995809	PrEC	prostate:	n/a
27	chr4:68929020-68929070	GM12891	blood:	n/a
28	chr4:68995995-68996045	SKMC	muscle:	n/a
29	chr4:68919575-68919625	HNPCEpiC	eye:	n/a
30	chr4:68930433-68930483	NT2-D1	testis:	n/a
31	chr4:68929020-68929070	HL-60	blood:	n/a
32	chr4:68995759-68995809	HepG2	liver:	n/a
33	chr4:68995759-68995809	HCF	heart:	n/a
34	chr4:68928981-68929031	HepG2	liver:	n/a
35	chr4:68995759-68995809	PANC-1	pancreas:	n/a
36	chr4:68930433-68930483	LNCaP	prostate:	n/a
37	chr4:68929413-68929463	NH-A	brain:	n/a
38	chr4:68995995-68996045	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:68928981-68929031	NB4	blood:	n/a
40	chr4:68995759-68995809	ProgFib	skin:	n/a
41	chr4:68930433-68930483	HIPEpiC	eye:	n/a
42	chr4:68919575-68919625	HEEpiC	esophagus:	n/a
43	chr4:68919575-68919625	A549	lung:	n/a
44	chr4:68995759-68995809	Caco-2	colon:	n/a
45	chr4:68995759-68995809	AG10803	skin:	n/a
46	chr4:68995995-68996045	HCF	heart:	n/a
47	chr4:68929413-68929463	SAEC	small airway:	n/a
48	chr4:68995759-68995809	NB4	blood:	n/a
49	chr4:68995759-68995809	IMR90	lung:	fetal
50	chr4:68930433-68930483	Hela-S3	cervix:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:68782884..68785601-chr4:68941722..68943617,2	MCF-7	breast:
2	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
3	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
4	chr4:68924336..68926843-chr4:68931083..68932839,2	MCF-7	breast:
5	chr4:68924336..68926843-chr4:68931083..68932839,2	MCF-7	breast:
6	chr4:68798924..68801314-chr4:68932123..68934294,2	MCF-7	breast:
7	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
8	chr4:68919044..68921969-chr4:68924326..68927015,2	K562	blood:
9	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
10	chr4:68945279..68946241-chr4:69040966..69041537,2	K562	blood:
11	chr11:73471645..73472154-chr4:68919136..68920088,2	MCF-7	breast:
12	chr4:69014952..69016678-chr4:69016935..69018473,2	K562	blood:
13	chr4:68588334..68590985-chr4:68982055..68983628,2	K562	blood:
14	chr4:68945761..68946581-chr4:69040992..69041794,2	MCF-7	breast:
15	chr4:68941684..68942576-chr4:69041048..69041788,2	K562	blood:
16	chr4:69012983..69014956-chr4:69018521..69020057,2	K562	blood:
17	chr4:68919044..68921969-chr4:68924326..68927015,2	K562	blood:
18	chr4:68941725..68942553-chr4:69040855..69041893,4	MCF-7	breast:
19	chr4:68913890..68916498-chr4:68916992..68918591,2	MCF-7	breast:
20	chr4:68854585..68857401-chr4:68944516..68946087,2	MCF-7	breast:
21	chr4:69012983..69014956-chr4:69018521..69020057,2	K562	blood:
22	chr4:68911783..68913982-chr4:68917527..68919121,2	K562	blood:
23	chr4:69014952..69016678-chr4:69016935..69018473,2	K562	blood:
24	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:
25	chr4:68994438..68997123-chr4:69006589..69008746,2	K562	blood:
26	chr4:68913890..68916498-chr4:68916992..68918591,2	MCF-7	breast:
27	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMPRSS11E-1	chr4:68926333-68928939	NONHSAT096719
2	lnc-TMPRSS11E-1	chr4:68928801-68928939	ENSG00000248049
3	lnc-TMPRSS11A-2	chr4:68928266-68928986	NONHSAT147287
4	lnc-TMPRSS11A-2	chr4:68927630-68929015	NONHSAT096720
5	lnc-TMPRSS11E-1	chr4:68938823-68938951	NONHSAT096719
6	lnc-TMPRSS11E-1	chr4:68919226-68919276	NONHSAT096719
7	lnc-TMPRSS11E-1	chr4:68942997-68943139	ENSG00000248049
8	lnc-TMPRSS11E-1	chr4:68945839-68946363	ENSG00000248049
9	lnc-TMPRSS11A-2	chr4:68926328-68927569	NONHSAT096721
10	lnc-TMPRSS11E-1	chr4:68943181-68943348	ENSG00000248049
11	lnc-TMPRSS11A-2	chr4:68926312-68926518	NONHSAT096720
12	lnc-TMPRSS11A-2	chr4:68927630-68929015	NONHSAT096721
13	lnc-TMPRSS11E-1	chr4:68928780-68928939	ENSG00000248049
14	lnc-TMPRSS11A-2	chr4:68926583-68927569	NONHSAT096720
15	lnc-TMPRSS11E-1	chr4:68945839-68945944	ENSG00000248049
16	lnc-TMPRSS11E-1	chr4:68928325-68928939	ENSG00000248049
17	lnc-TMPRSS11E-1	chr4:68945839-68946670	ENSG00000248049
18	lnc-TMPRSS11A-2	chr4:68927540-68928987	NONHSAT096722

No data

Variant related genes	Relation type
SYT14L	TF binding region
UBA6-AS1	TF binding region
TMPRSS11F	TF binding region
SYT14L	CpG island
UBA6-AS1	CpG island
TMPRSS11F	CpG island
ENSG00000175582	chromatin interactions
ENSG00000270228	chromatin interactions
ENSG00000198092	chromatin interactions
ASPH	miRNA target sites
BCL2L11	miRNA target sites
BRD1	miRNA target sites
GOLGA6A	miRNA target sites
KLHL15	miRNA target sites
DICER1	miRNA target sites
DDX50	miRNA target sites
RALGPS2	miRNA target sites

Extended variants
information (count: 2419 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2419 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13112221	chr4:68915798-68915799	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569888455	chr4:68915821-68915822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140233410	chr4:68915871-68915872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs13132100	chr4:68915886-68915887	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs181893779	chr4:68915918-68915919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540896591	chr4:68915923-68915924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34058514	chr4:68916080-68916081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7684825	chr4:68916096-68916097	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs566167048	chr4:68916145-68916146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369215813	chr4:68916170-68916171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372833098	chr4:68916180-68916181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144011251	chr4:68916200-68916201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186537324	chr4:68916235-68916236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551059061	chr4:68916240-68916241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571209412	chr4:68916284-68916285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377189590	chr4:68916323-68916324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1866327	chr4:68916329-68916330	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs554031339	chr4:68916330-68916331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567509375	chr4:68916334-68916335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536412425	chr4:68916337-68916338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189757795	chr4:68916342-68916343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1866328	chr4:68916358-68916359	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs575772793	chr4:68916412-68916413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369471425	chr4:68916463-68916464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146423829	chr4:68916464-68916465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577940681	chr4:68916466-68916467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557895249	chr4:68916541-68916542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149104196	chr4:68916581-68916582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1866329	chr4:68916583-68916584	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs557615606	chr4:68916676-68916677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182655932	chr4:68916704-68916705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573897712	chr4:68916720-68916721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542786738	chr4:68916722-68916723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373154699	chr4:68916796-68916797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188127691	chr4:68916798-68916799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12645384	chr4:68916846-68916847	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs6812743	chr4:68916865-68916866	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs191224326	chr4:68916873-68916874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147506210	chr4:68916884-68916885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12643306	chr4:68916887-68916888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12651598	chr4:68916898-68916899	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs11131735	chr4:68916907-68916908	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs11947862	chr4:68916948-68916949	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs532928014	chr4:68916956-68916957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549541152	chr4:68916958-68916959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374601701	chr4:68916975-68916976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74916112	chr4:68916983-68916984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563569266	chr4:68917006-68917007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529243443	chr4:68917010-68917011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11947869	chr4:68917026-68917027	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:94)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Alcoholism	21790672	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Autism	19287141	CNVD

Chromatin state (count:153 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68915600-68916600	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr4:68915800-68916600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:68915800-68916600	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr4:68916600-68920000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr4:68916600-68920000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr4:68916600-68920400	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr4:68916800-68920200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr4:68920000-68920800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr4:68920000-68921000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr4:68920000-68921200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr4:68920200-68920800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr4:68920400-68921000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr4:68920400-68921200	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr4:68920600-68921200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr4:68927400-68929000	Active TSS	Brain Anterior Caudate	brain
16	chr4:68927600-68928600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr4:68928000-68928800	Active TSS	Brain Angular Gyrus	brain
18	chr4:68928000-68928800	Active TSS	Brain Cingulate Gyrus	brain
19	chr4:68928000-68928800	Active TSS	Brain Inferior Temporal Lobe	brain
20	chr4:68928000-68929000	Active TSS	Brain Hippocampus Middle	brain
21	chr4:68928200-68928600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
22	chr4:68928200-68928600	Active TSS	K562	blood
23	chr4:68928200-68928800	Active TSS	Brain Substantia Nigra	brain
24	chr4:68932200-68943600	Weak transcription	Esophagus	oesophagus
25	chr4:68936000-68936600	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr4:68936000-68939400	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr4:68936200-68936400	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr4:68936200-68936800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr4:68936400-68936600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr4:68936400-68938400	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr4:68936600-68937400	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr4:68936800-68938000	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr4:68937200-68938200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr4:68937400-68939600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr4:68938000-68939600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr4:68938200-68938400	Bivalent/Poised TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr4:68938200-68938600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr4:68938200-68939000	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr4:68938200-68939600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:68938200-68939600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr4:68938200-68939600	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr4:68938400-68938800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr4:68938600-68939000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:68938600-68939400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr4:68938800-68939400	Enhancers	H1 Cell Line	embryonic stem cell
46	chr4:68939000-68939600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:68940000-68940400	Enhancers	NHEK	skin
48	chr4:68940400-68941000	Enhancers	HMEC	breast
49	chr4:68940400-68941200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr4:68940400-68941200	Enhancers	Placenta	Placenta

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