Variant report

Variant	nsv1012379
Chromosome Location	chr4:85071268-85205732
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1121)
CpG islands
(count:429)
Chromatin interactive
region (count:29)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1121 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:85201066-85201147	K562	blood:	n/a	n/a
2	ATF1	chr4:85158186-85158535	K562	blood:	n/a	n/a
3	ATF1	chr4:85178825-85179057	K562	blood:	n/a	n/a
4	ATF1	chr4:85165754-85165952	K562	blood:	n/a	n/a
5	ATF1	chr4:85152699-85153034	K562	blood:	n/a	n/a
6	ATF2	chr4:85180433-85180723	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:85156731-85157066	GM12878	blood:	n/a	n/a
8	ATF3	chr4:85158247-85158485	K562	blood:	n/a	n/a
9	BACH1	chr4:85200981-85201146	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr4:85180074-85180335	GM12878	blood:	n/a	chr4:85180194-85180205
11	BATF	chr4:85180048-85180299	GM12878	blood:	n/a	chr4:85180194-85180205
12	BHLHE40	chr4:85152697-85152993	K562	blood:	n/a	n/a
13	BHLHE40	chr4:85165637-85165726	K562	blood:	n/a	n/a
14	BHLHE40	chr4:85158275-85158640	K562	blood:	n/a	n/a
15	CBX3	chr4:85181689-85182115	HCT-116	colon:	n/a	n/a
16	CBX3	chr4:85088813-85089099	HCT-116	colon:	n/a	n/a
17	CEBPB	chr4:85199121-85199340	MCF-7	breast:	n/a	n/a
18	CEBPB	chr4:85108449-85108714	H1-hESC	embryonic stem cell:	n/a	chr4:85108566-85108577
19	CEBPB	chr4:85119744-85120477	HepG2	liver:	n/a	chr4:85119904-85119915
20	CEBPB	chr4:85175712-85176074	IMR90	lung:	n/a	chr4:85175883-85175894
21	CEBPB	chr4:85159385-85159752	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:85148336-85148471	HepG2	liver:	n/a	chr4:85148391-85148402
23	CEBPB	chr4:85079965-85080234	A549	lung:	n/a	n/a
24	CEBPB	chr4:85108520-85108554	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:85205499-85205733	A549	lung:	n/a	chr4:85205587-85205598 chr4:85205586-85205597
26	CEBPB	chr4:85079993-85080193	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:85199101-85199458	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:85175715-85176027	A549	lung:	n/a	chr4:85175883-85175894
29	CEBPB	chr4:85199084-85199512	K562	blood:	n/a	n/a
30	CEBPB	chr4:85148398-85148410	K562	blood:	n/a	n/a
31	CEBPB	chr4:85135969-85136221	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:85159377-85159684	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr4:85163236-85163510	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:85205579-85205730	K562	blood:	n/a	chr4:85205587-85205598 chr4:85205586-85205597
35	CEBPB	chr4:85199051-85199470	A549	lung:	n/a	n/a
36	CEBPB	chr4:85080088-85080249	IMR90	lung:	n/a	n/a
37	CEBPB	chr4:85175724-85176062	K562	blood:	n/a	chr4:85175883-85175894
38	CEBPB	chr4:85199102-85199389	MCF-7	breast:	n/a	n/a
39	CEBPB	chr4:85119744-85120069	IMR90	lung:	n/a	chr4:85119904-85119915
40	CEBPB	chr4:85205495-85205761	HepG2	liver:	n/a	chr4:85205587-85205598 chr4:85205586-85205597
41	CEBPB	chr4:85205456-85205743	IMR90	lung:	n/a	chr4:85205587-85205598 chr4:85205586-85205597
42	CEBPB	chr4:85199113-85199436	A549	lung:	n/a	n/a
43	CEBPB	chr4:85199108-85199414	K562	blood:	n/a	n/a
44	CEBPB	chr4:85199104-85199472	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr4:85119769-85120419	A549	lung:	n/a	chr4:85119904-85119915
46	CEBPB	chr4:85175743-85175944	H1-hESC	embryonic stem cell:	n/a	chr4:85175883-85175894
47	CEBPB	chr4:85199145-85199350	K562	blood:	n/a	n/a
48	CEBPB	chr4:85084572-85084750	HepG2	liver:	n/a	chr4:85084721-85084730 chr4:85084719-85084730
49	CEBPB	chr4:85156460-85156708	H1-hESC	embryonic stem cell:	n/a	chr4:85156584-85156595
50	CEBPB	chr4:85135957-85136188	A549	lung:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:85205711-85205761	AG10803	skin:	n/a
2	chr4:85163562-85163612	CMK	blood:	n/a
3	chr4:85205711-85205761	AG10803	skin:	n/a
4	chr4:85163562-85163612	CMK	blood:	n/a
5	chr4:85165689-85165739	Caco-2	colon:	n/a
6	chr4:85139232-85139282	U87	brain:	n/a
7	chr4:85165689-85165739	SK-N-SH_RA	brain:	n/a
8	chr4:85205711-85205761	SAEC	small airway:	n/a
9	chr4:85145324-85145374	GM06990	blood:	n/a
10	chr4:85205711-85205761	GM12892	blood:	n/a
11	chr4:85076551-85076601	GM12892	blood:	n/a
12	chr4:85139232-85139282	A549	lung:	n/a
13	chr4:85163562-85163612	MCF10A-Er-Src	breast:	n/a
14	chr4:85139232-85139282	AG10803	skin:	n/a
15	chr4:85163562-85163612	HL-60	blood:	n/a
16	chr4:85145324-85145374	RPTEC	kidney:	n/a
17	chr4:85163562-85163612	K562	blood:	n/a
18	chr4:85145324-85145374	ovcar-3	ovarian:	n/a
19	chr4:85139232-85139282	NHDF-neo	bronchial:	n/a
20	chr4:85163562-85163612	HEEpiC	esophagus:	n/a
21	chr4:85139232-85139282	GM12892	blood:	n/a
22	chr4:85165491-85165541	T-47D	breast:	n/a
23	chr4:85145324-85145374	Hela-S3	cervix:	n/a
24	chr4:85076551-85076601	HRE	kidney:	n/a
25	chr4:85165689-85165739	GM19239	blood:	n/a
26	chr4:85139232-85139282	Caco-2	colon:	n/a
27	chr4:85165689-85165739	HEK293	kidney:	embryo
28	chr4:85163562-85163612	Hepatocyte	liver:	n/a
29	chr4:85165491-85165541	AG09319	gingival:	n/a
30	chr4:85165689-85165739	NHDF-neo	bronchial:	n/a
31	chr4:85165689-85165739	NT2-D1	testis:	n/a
32	chr4:85139232-85139282	NT2-D1	testis:	n/a
33	chr4:85165689-85165739	AG04449	skin:	fetal
34	chr4:85163562-85163612	LNCaP	prostate:	n/a
35	chr4:85163562-85163612	NHBE	bronchial:	n/a
36	chr4:85165491-85165541	SAEC	small airway:	n/a
37	chr4:85163562-85163612	H1-hESC	embryonic stem cell:	embryo
38	chr4:85165689-85165739	LNCaP	prostate:	n/a
39	chr4:85165689-85165739	SK-N-SH	brain:	n/a
40	chr4:85163562-85163612	NHDF-neo	bronchial:	n/a
41	chr4:85145324-85145374	HAEpiC	amniotic membrane:	n/a
42	chr4:85076551-85076601	HCF	heart:	n/a
43	chr4:85165491-85165541	H1-hESC	embryonic stem cell:	embryo
44	chr4:85165491-85165541	HNPCEpiC	eye:	n/a
45	chr4:85205711-85205761	IMR90	lung:	fetal
46	chr4:85076551-85076601	AoSMC	blood vessel:	n/a
47	chr4:85139232-85139282	SK-N-MC	brain:	n/a
48	chr4:85145324-85145374	IMR90	lung:	fetal
49	chr4:85165689-85165739	NB4	blood:	n/a
50	chr4:85205711-85205761	AG09319	gingival:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:85080575..85081559-chr4:85180120..85181416,6	MCF-7	breast:
2	chr4:85143338..85145421-chr4:85146842..85148891,2	K562	blood:
3	chr4:85174053..85178031-chr4:85178404..85182259,4	K562	blood:
4	chr4:85159698..85160208-chr4:85372408..85372912,2	MCF-7	breast:
5	chr4:85198661..85201031-chr4:85203402..85205789,2	K562	blood:
6	chr4:85072451..85073423-chr4:85180134..85180901,4	MCF-7	breast:
7	chr4:85103034..85104935-chr4:85113026..85114643,2	K562	blood:
8	chr4:85191697..85192557-chr4:85372441..85373864,5	MCF-7	breast:
9	chr4:85103034..85104935-chr4:85113026..85114643,2	K562	blood:
10	chr4:85139303..85141304-chr4:85144022..85145808,2	K562	blood:
11	chr4:85143892..85145421-chr4:85147391..85149801,2	K562	blood:
12	chr4:84882460..84883415-chr4:85088632..85089152,2	MCF-7	breast:
13	chr4:85072631..85073368-chr4:85450368..85450912,2	MCF-7	breast:
14	chr4:85080701..85081585-chr4:85425136..85425979,2	MCF-7	breast:
15	chr4:85143338..85145421-chr4:85146842..85148891,2	K562	blood:
16	chr4:85080575..85081559-chr4:85180120..85181416,6	MCF-7	breast:
17	chr4:85071031..85073190-chr4:85079864..85082804,2	MCF-7	breast:
18	chr4:84827046..84827675-chr4:85088517..85089246,2	MCF-7	breast:
19	chr4:85071031..85073190-chr4:85079864..85082804,2	MCF-7	breast:
20	chr4:84565617..84566470-chr4:85088713..85089282,2	MCF-7	breast:
21	chr4:85174053..85178031-chr4:85178404..85182259,4	K562	blood:
22	chr4:85139303..85141304-chr4:85144022..85145808,2	K562	blood:
23	chr20:52481552..52482195-chr4:85078491..85079377,2	MCF-7	breast:
24	chr4:85200318..85202526-chr4:85203716..85205846,2	MCF-7	breast:
25	chr4:85072431..85073209-chr4:85424476..85425190,3	MCF-7	breast:
26	chr4:85072451..85073423-chr4:85180134..85180901,4	MCF-7	breast:
27	chr4:85194924..85197850-chr4:85199277..85201015,2	K562	blood:
28	chr4:85143892..85145421-chr4:85147391..85149801,2	K562	blood:
29	chr4:85194924..85197850-chr4:85199277..85201015,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NKX6-1-3	chr4:85152232-85152296	ucscGeneNc_uc010ikd_1
2	lnc-NKX6-1-2	chr4:85205359-85205480	NONHSAT097229
3	lnc-NKX6-1-3	chr4:85075800-85075907	ucscGeneNc_uc010ikd_1
4	lnc-NKX6-1-2	chr4:85205359-85205479	ENSG00000250546
5	lnc-NKX6-1-2	chr4:85164264-85164369	ENSG00000250546
6	lnc-NKX6-1-2	chr4:85164264-85164369	NONHSAT097229

No data

Variant related genes	Relation type
ENSG00000250546	TF binding region
RNU6-774P	TF binding region
ENSG00000214980	TF binding region
ENSG00000250546	CpG island
RNU6-774P	CpG island
ENSG00000214980	CpG island
ENSG00000250546	chromatin interactions
DYRK2	miRNA target sites
FAM3C	miRNA target sites

Extended variants
information (count: 2609 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2609 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576548680	chr4:85071465-85071466	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs543657445	chr4:85071510-85071511	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs58579033	chr4:85071519-85071520	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs532903773	chr4:85071611-85071612	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs552351114	chr4:85071614-85071615	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs559751983	chr4:85071618-85071619	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs527306292	chr4:85071635-85071636	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs111730690	chr4:85071655-85071656	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs373509337	chr4:85072600-85072601	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs548334480	chr4:85072605-85072606	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs2178604	chr4:85072631-85072632	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs537380081	chr4:85072648-85072649	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs114854783	chr4:85072685-85072686	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs144497236	chr4:85072698-85072699	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs534892265	chr4:85072714-85072715	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs538081072	chr4:85072717-85072718	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs369093263	chr4:85072748-85072749	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs201866288	chr4:85072766-85072767	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs145433720	chr4:85072774-85072775	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs149219624	chr4:85072785-85072786	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs560753248	chr4:85072807-85072808	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs143006731	chr4:85072841-85072842	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs555126077	chr4:85072853-85072854	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs78017984	chr4:85072855-85072856	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs565197511	chr4:85072856-85072857	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs116641643	chr4:85072909-85072910	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs148198350	chr4:85072913-85072914	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs559787419	chr4:85072922-85072923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs141203601	chr4:85072923-85072924	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs540520040	chr4:85072934-85072935	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs1997478	chr4:85072970-85072971	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs1997477	chr4:85073083-85073084	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs537475716	chr4:85073145-85073146	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs552408696	chr4:85073146-85073147	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs570819828	chr4:85073202-85073203	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs572235030	chr4:85075816-85075817	Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
37	rs75257767	chr4:85075817-85075818	Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
38	rs139692771	chr4:85075850-85075851	Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
39	rs533239736	chr4:85075861-85075862	Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
40	rs372075719	chr4:85075863-85075864	Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
41	rs116642903	chr4:85075876-85075877	Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
42	rs535129700	chr4:85075911-85075912	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs12643400	chr4:85075937-85075938	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs183878010	chr4:85075941-85075942	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs76091332	chr4:85076066-85076067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557575632	chr4:85076131-85076132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs376722691	chr4:85076132-85076133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73833657	chr4:85076133-85076134	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs190549551	chr4:85076154-85076155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs371691523	chr4:85076161-85076162	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	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
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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Prostate cancer	16573809	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:194 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:85075800-85076000	Bivalent Enhancer	Fetal Lung	lung
2	chr4:85075800-85076800	Enhancers	H1 Cell Line	embryonic stem cell
3	chr4:85075800-85076800	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr4:85075800-85077000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr4:85076000-85076600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr4:85076000-85076800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:85076000-85076800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr4:85076000-85077000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr4:85076000-85077000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:85076200-85076800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr4:85076400-85076800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr4:85076400-85077000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr4:85076800-85080400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr4:85077000-85078200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr4:85078600-85078800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr4:85079000-85079600	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr4:85079000-85080000	Enhancers	Fetal Intestine Small	intestine
18	chr4:85079200-85080400	Enhancers	Fetal Intestine Large	intestine
19	chr4:85079600-85080200	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr4:85079800-85081200	Bivalent Enhancer	Fetal Lung	lung
21	chr4:85080000-85080400	Active TSS	Fetal Intestine Small	intestine
22	chr4:85080200-85080400	Active TSS	Duodenum Mucosa	Duodenum
23	chr4:85080200-85080600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr4:85080400-85080600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr4:85080400-85080600	Flanking Active TSS	Duodenum Mucosa	Duodenum
26	chr4:85080400-85080600	Flanking Active TSS	Fetal Intestine Large	intestine
27	chr4:85080400-85084000	Enhancers	Fetal Intestine Small	intestine
28	chr4:85080600-85080800	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr4:85080600-85081800	Enhancers	Fetal Intestine Large	intestine
30	chr4:85081800-85083400	Weak transcription	Fetal Intestine Large	intestine
31	chr4:85083200-85086400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:85083400-85083600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr4:85083400-85084000	Enhancers	Fetal Intestine Large	intestine
34	chr4:85083600-85084000	Bivalent Enhancer	Dnd41	blood
35	chr4:85085000-85085400	Enhancers	Fetal Lung	lung
36	chr4:85086400-85086600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr4:85086400-85086600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr4:85086400-85086800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr4:85086600-85088600	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr4:85086600-85088600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr4:85088600-85089200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr4:85088600-85089400	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr4:85091200-85091400	Bivalent Enhancer	Fetal Lung	lung
44	chr4:85091400-85093000	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr4:85093200-85093400	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr4:85099200-85099600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr4:85108400-85108800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr4:85108600-85109200	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr4:85108600-85109200	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr4:85109600-85110600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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