Variant report

Variant	nsv1013602
Chromosome Location	chr4:78133566-78217004
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	ATF1	chr4:78153907-78154134	K562	blood:	n/a	n/a
2	BATF	chr4:78140257-78140528	GM12878	blood:	n/a	chr4:78140400-78140410 chr4:78140399-78140410
3	BHLHE40	chr4:78161829-78161910	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:78169965-78170247	HepG2	liver:	n/a	n/a
5	BHLHE40	chr4:78161695-78162114	K562	blood:	n/a	n/a
6	BRCA1	chr4:78161761-78161808	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:78142599-78142677	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr4:78161727-78161966	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr4:78215423-78215638	IMR90	lung:	n/a	chr4:78215544-78215555
10	CEBPB	chr4:78136939-78137228	A549	lung:	n/a	chr4:78137093-78137104
11	CEBPB	chr4:78136969-78137231	HepG2	liver:	n/a	chr4:78137093-78137104
12	CEBPB	chr4:78142460-78142826	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:78171884-78171912	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:78142464-78142815	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:78215392-78215580	K562	blood:	n/a	chr4:78215544-78215555
16	CEBPB	chr4:78169257-78169440	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:78215400-78215689	HepG2	liver:	n/a	chr4:78215544-78215555
18	CTCF	chr4:78149260-78149410	GM12801	blood:	n/a	chr4:78149335-78149353
19	CTCF	chr4:78161740-78161890	HRE	kidney:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
20	CTCF	chr4:78161613-78162043	IMR90	lung:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
21	CTCF	chr4:78161620-78161910	A549	lung:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
22	CTCF	chr4:78149260-78149410	MCF-7	breast:	n/a	chr4:78149335-78149353
23	CTCF	chr4:78156520-78156670	GM12873	blood:	n/a	n/a
24	CTCF	chr4:78198600-78198750	GM12873	blood:	n/a	chr4:78198641-78198650
25	CTCF	chr4:78161666-78161954	MCF-7	breast:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
26	CTCF	chr4:78188140-78188290	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr4:78161760-78161910	GM12865	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
28	CTCF	chr4:78162040-78162190	AG04449	skin:	n/a	n/a
29	CTCF	chr4:78161740-78161890	GM06990	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
30	CTCF	chr4:78161697-78161941	GM10248	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
31	CTCF	chr4:78161740-78161890	GM12878	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
32	CTCF	chr4:78161760-78161910	HPAF	blood vessel:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
33	CTCF	chr4:78170600-78170750	HBMEC	blood vessel:	n/a	chr4:78170664-78170685 chr4:78170669-78170687 chr4:78170675-78170684
34	CTCF	chr4:78197240-78197390	HepG2	liver:	n/a	n/a
35	CTCF	chr4:78170600-78170750	HMF	breast:	n/a	chr4:78170664-78170685 chr4:78170669-78170687 chr4:78170675-78170684
36	CTCF	chr4:78161681-78161953	H1-hESC	embryonic stem cell:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
37	CTCF	chr4:78170640-78170790	HVMF	connective:	n/a	chr4:78170664-78170685 chr4:78170669-78170687 chr4:78170675-78170684
38	CTCF	chr4:78161380-78161530	GM12864	blood:	n/a	n/a
39	CTCF	chr4:78148120-78148270	HCT-116	colon:	n/a	n/a
40	CTCF	chr4:78161780-78161930	GM12866	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
41	CTCF	chr4:78161690-78161962	GM13977	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
42	CTCF	chr4:78161760-78161910	GM12867	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
43	CTCF	chr4:78161689-78161957	Pancreas_OC	pancreas:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
44	CTCF	chr4:78161060-78161210	AG10803	skin:	n/a	n/a
45	CTCF	chr4:78161582-78162152	HCT-116	colon:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
46	CTCF	chr4:78170540-78170690	HCT-116	colon:	n/a	chr4:78170664-78170685 chr4:78170669-78170687 chr4:78170675-78170684
47	CTCF	chr4:78161760-78161910	GM12875	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
48	CTCF	chr4:78161720-78161870	K562	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
49	CTCF	chr4:78149300-78149450	HMF	breast:	n/a	chr4:78149335-78149353
50	CTCF	chr4:78165220-78165370	GM12875	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78156196-78156246	Hepatocyte	liver:	n/a
2	chr4:78156196-78156246	HMEC	breast:	n/a
3	chr4:78156196-78156246	HepG2	liver:	n/a
4	chr4:78156196-78156246	HCPEpiC	choroid plexus:	n/a
5	chr4:78156196-78156246	CMK	blood:	n/a
6	chr4:78156196-78156246	ECC-1	luminal epithelium:	n/a
7	chr4:78156196-78156246	NB4	blood:	n/a
8	chr4:78156196-78156246	AG09319	gingival:	n/a
9	chr4:78156196-78156246	HAEpiC	amniotic membrane:	n/a
10	chr4:78156196-78156246	H1-hESC	embryonic stem cell:	embryo
11	chr4:78156196-78156246	IMR90	lung:	fetal
12	chr4:78156196-78156246	PANC-1	pancreas:	n/a
13	chr4:78156196-78156246	HEEpiC	esophagus:	n/a
14	chr4:78156196-78156246	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:78156196-78156246	NHBE	bronchial:	n/a
16	chr4:78156196-78156246	RPTEC	kidney:	n/a
17	chr4:78156196-78156246	LNCaP	prostate:	n/a
18	chr4:78156196-78156246	HRCEpiC	kidney:	n/a
19	chr4:78156196-78156246	BJ	skin:	n/a
20	chr4:78156196-78156246	HCT-116	colon:	n/a
21	chr4:78156196-78156246	ovcar-3	ovarian:	n/a
22	chr4:78156196-78156246	BE2_C	brain:	n/a
23	chr4:78156196-78156246	NH-A	brain:	n/a
24	chr4:78156196-78156246	AG04450	lung:	fetal
25	chr4:78156196-78156246	HUVEC	blood vessel:	n/a
26	chr4:78156196-78156246	GM06990	blood:	n/a
27	chr4:78156196-78156246	SK-N-SH	brain:	n/a
28	chr4:78156196-78156246	Caco-2	colon:	n/a
29	chr4:78156196-78156246	U87	brain:	n/a
30	chr4:78156196-78156246	SK-N-MC	brain:	n/a
31	chr4:78156196-78156246	ProgFib	skin:	n/a
32	chr4:78156196-78156246	GM12878	blood:	n/a
33	chr4:78156196-78156246	HIPEpiC	eye:	n/a
34	chr4:78156196-78156246	PFSK-1	brain:	n/a
35	chr4:78156196-78156246	AG09309	skin:	n/a
36	chr4:78156196-78156246	HL-60	blood:	n/a
37	chr4:78156196-78156246	A549	lung:	n/a
38	chr4:78156196-78156246	NT2-D1	testis:	n/a
39	chr4:78156196-78156246	SAEC	small airway:	n/a
40	chr4:78156196-78156246	HEK293	kidney:	embryo
41	chr4:78156196-78156246	K562	blood:	n/a
42	chr4:78156196-78156246	SK-N-SH_RA	brain:	n/a
43	chr4:78156196-78156246	AoSMC	blood vessel:	n/a
44	chr4:78156196-78156246	GM12892	blood:	n/a
45	chr4:78156196-78156246	AG04449	skin:	fetal
46	chr4:78156196-78156246	HRE	kidney:	n/a
47	chr4:78156196-78156246	NHDF-neo	bronchial:	n/a
48	chr4:78156196-78156246	PrEC	prostate:	n/a
49	chr4:78156196-78156246	AG10803	skin:	n/a
50	chr4:78156196-78156246	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:78130169..78132632-chr4:78133437..78136630,3	K562	blood:
2	chr4:78161473..78162127-chr4:78394685..78395318,2	K562	blood:
3	chr4:78161721..78162270-chr4:78279119..78279681,2	MCF-7	breast:
4	chr4:78162165..78163774-chr4:78227168..78228953,2	MCF-7	breast:
5	chr4:78161365..78162334-chr4:78279195..78280134,7	K562	blood:
6	chr4:78149304..78151645-chr4:78154973..78157716,3	K562	blood:
7	chr4:78160754..78162321-chr4:78226906..78228617,2	MCF-7	breast:
8	chr4:78155142..78157870-chr4:78168469..78170209,2	MCF-7	breast:
9	chr4:78132153..78134677-chr4:78134780..78136645,2	MCF-7	breast:
10	chr4:78174499..78176837-chr4:78205161..78207032,2	MCF-7	breast:
11	chr4:78161324..78162321-chr4:78279149..78280134,4	MCF-7	breast:
12	chr4:78161284..78162458-chr4:78229777..78230742,7	K562	blood:
13	chr4:78149304..78151645-chr4:78154973..78157716,3	K562	blood:
14	chr4:78016602..78017111-chr4:78134180..78134764,2	MCF-7	breast:
15	chr4:78177354..78179710-chr4:78180664..78183643,2	MCF-7	breast:
16	chr4:78161398..78162211-chr4:78229720..78230660,3	MCF-7	breast:
17	chr4:78177354..78179710-chr4:78180664..78183643,2	MCF-7	breast:
18	chr4:77994973..77997901-chr4:78150275..78153619,3	MCF-7	breast:
19	chr4:78158067..78160012-chr4:78227264..78228770,2	MCF-7	breast:
20	chr4:78182930..78185790-chr4:78187841..78189605,2	K562	blood:
21	chr4:78161188..78162532-chr4:78229476..78230856,15	MCF-7	breast:
22	chr4:78016448..78019261-chr4:78148834..78151500,2	MCF-7	breast:
23	chr4:78161416..78162110-chr4:78226527..78227315,3	MCF-7	breast:
24	chr4:78132153..78134677-chr4:78134780..78136645,2	MCF-7	breast:
25	chr4:78182930..78185790-chr4:78187841..78189605,2	K562	blood:
26	chr4:78161311..78162711-chr4:78226629..78227614,14	MCF-7	breast:
27	chr4:78155252..78157365-chr4:78224145..78227144,3	MCF-7	breast:
28	chr4:78155142..78157870-chr4:78168469..78170209,2	MCF-7	breast:
29	chr4:78174499..78176837-chr4:78205161..78207032,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCNI-4	chr4:78137569-78138031	NONHSAT097051

Variant related genes	Relation type
ENSG00000270669	TF binding region
ENSG00000270669	CpG island
ENSG00000118816	chromatin interactions

Extended variants
information (count: 3655 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3655 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1006042	chr4:78133566-78133567	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551889179	chr4:78133569-78133570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569093215	chr4:78133590-78133591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531524357	chr4:78133607-78133608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548339225	chr4:78133617-78133618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568245069	chr4:78133622-78133623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146089221	chr4:78133665-78133666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371851156	chr4:78133666-78133667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554303787	chr4:78133679-78133680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550437718	chr4:78133690-78133691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372014016	chr4:78133691-78133692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570961091	chr4:78133692-78133693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539777352	chr4:78133703-78133704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534937958	chr4:78133704-78133705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576645284	chr4:78133732-78133733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542135151	chr4:78133785-78133786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs180707116	chr4:78133805-78133806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572298445	chr4:78133816-78133817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577602635	chr4:78133839-78133840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185910299	chr4:78133867-78133868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190025290	chr4:78133896-78133897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532086953	chr4:78133994-78133995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs111274298	chr4:78133997-78133998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114054717	chr4:78133998-78133999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113587683	chr4:78134107-78134108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143075952	chr4:78134113-78134114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548176849	chr4:78134148-78134149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148233213	chr4:78134152-78134153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375098143	chr4:78134178-78134179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547622649	chr4:78134179-78134180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112951586	chr4:78134207-78134208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558610545	chr4:78134225-78134226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539568957	chr4:78134233-78134234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556644093	chr4:78134239-78134240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182586009	chr4:78134318-78134319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368368697	chr4:78134370-78134371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573743826	chr4:78134418-78134419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs59160085	chr4:78134444-78134445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569855188	chr4:78134445-78134446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs115764924	chr4:78134453-78134454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187290676	chr4:78134455-78134456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141127540	chr4:78134477-78134478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536903366	chr4:78134578-78134579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190513821	chr4:78134616-78134617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183534949	chr4:78134621-78134622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562642983	chr4:78134622-78134623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575943476	chr4:78134662-78134663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541812593	chr4:78134665-78134666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542855700	chr4:78134693-78134694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372450564	chr4:78134727-78134728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78125200-78143600	Weak transcription	Primary B cells from cord blood	blood
2	chr4:78135200-78135400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:78135200-78135400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:78136200-78136800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:78136400-78136600	Enhancers	Fetal Heart	heart
6	chr4:78136400-78136800	Enhancers	Fetal Muscle Leg	muscle
7	chr4:78136600-78139600	Weak transcription	Fetal Heart	heart
8	chr4:78136800-78139200	Weak transcription	Fetal Muscle Leg	muscle
9	chr4:78139200-78140600	Enhancers	Fetal Muscle Leg	muscle
10	chr4:78139600-78140000	Enhancers	Fetal Heart	heart
11	chr4:78140000-78140200	Weak transcription	Fetal Heart	heart
12	chr4:78140200-78144000	Enhancers	Fetal Heart	heart
13	chr4:78140600-78141800	Weak transcription	Fetal Muscle Leg	muscle
14	chr4:78141800-78142800	Enhancers	Fetal Muscle Leg	muscle
15	chr4:78141800-78143200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:78142000-78143000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:78142000-78143000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:78142200-78142400	Enhancers	Aorta	Aorta
19	chr4:78142200-78142800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:78142200-78142800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr4:78142200-78143200	Bivalent Enhancer	Osteobl	bone
22	chr4:78142400-78142600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr4:78142600-78143200	Enhancers	Fetal Lung	lung
24	chr4:78142800-78145600	Weak transcription	Fetal Muscle Leg	muscle
25	chr4:78143200-78143400	Enhancers	Aorta	Aorta
26	chr4:78143200-78143400	Enhancers	Fetal Muscle Trunk	muscle
27	chr4:78145600-78147200	Enhancers	Fetal Muscle Leg	muscle
28	chr4:78146000-78146200	Enhancers	Fetal Muscle Trunk	muscle
29	chr4:78146000-78146600	Enhancers	Right Atrium	heart
30	chr4:78146000-78147400	Enhancers	Fetal Heart	heart
31	chr4:78146200-78147800	Weak transcription	Fetal Muscle Trunk	muscle
32	chr4:78147400-78152200	Weak transcription	Fetal Heart	heart
33	chr4:78147600-78148000	Weak transcription	Primary B cells from cord blood	blood
34	chr4:78147800-78148800	ZNF genes & repeats	Fetal Muscle Trunk	muscle
35	chr4:78148000-78149000	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr4:78148600-78148800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr4:78148600-78148800	Enhancers	HMEC	breast
38	chr4:78148800-78153600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:78149000-78156400	Weak transcription	Primary B cells from cord blood	blood
40	chr4:78149200-78150400	Weak transcription	HMEC	breast
41	chr4:78150000-78150800	Enhancers	Esophagus	oesophagus
42	chr4:78150000-78151000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr4:78150400-78151200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:78150400-78151200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr4:78150400-78151400	Enhancers	HMEC	breast
46	chr4:78150400-78151400	Enhancers	NHEK	skin
47	chr4:78150800-78153400	Weak transcription	Esophagus	oesophagus
48	chr4:78151200-78153600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr4:78152200-78153400	Enhancers	Fetal Heart	heart
50	chr4:78152400-78156000	Weak transcription	Primary T cells from cord blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links