Variant report

Variant	esv1802071
Chromosome Location	chr4:76948817-76972594
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	ATF2	chr4:76963311-76963770	GM12878	blood:	n/a	n/a
2	ATF2	chr4:76963342-76963708	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:76956439-76956654	GM12878	blood:	n/a	n/a
4	CEBPB	chr4:76959264-76959277	K562	blood:	n/a	n/a
5	CEBPB	chr4:76959131-76959345	HepG2	liver:	n/a	chr4:76959251-76959262
6	CEBPB	chr4:76949796-76950104	Hela-S3	cervix:	n/a	chr4:76949866-76949878
7	CHD2	chr4:76961734-76962547	K562	blood:	n/a	n/a
8	CTCF	chr4:76958172-76958198	GM19238	blood:	n/a	n/a
9	CTCF	chr4:76958140-76958290	HepG2	liver:	n/a	n/a
10	CTCF	chr4:76958076-76958325	NHEK	skin:	n/a	n/a
11	CTCF	chr4:76958150-76958153	MCF-7	breast:	n/a	n/a
12	CTCF	chr4:76958200-76958350	HEEpiC	esophagus:	n/a	n/a
13	CTCF	chr4:76958140-76958290	HEEpiC	esophagus:	n/a	n/a
14	CTCF	chr4:76957941-76958324	K562	blood:	n/a	n/a
15	CTCF	chr4:76958061-76958354	K562	blood:	n/a	n/a
16	CTCF	chr4:76956300-76956450	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr4:76958006-76958289	K562	blood:	n/a	n/a
18	CTCF	chr4:76958136-76958208	MCF-7	breast:	n/a	n/a
19	CTCF	chr4:76958200-76958248	HepG2	liver:	n/a	n/a
20	CTCF	chr4:76958058-76958376	K562	blood:	n/a	n/a
21	CTCF	chr4:76958154-76958245	MCF-7	breast:	n/a	n/a
22	CTCF	chr4:76960275-76960308	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr4:76958120-76958270	GM12866	blood:	n/a	n/a
24	CTCF	chr4:76958140-76958290	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr4:76958134-76958285	K562	blood:	n/a	n/a
26	CTCF	chr4:76956980-76957130	AG10803	skin:	n/a	n/a
27	CTCF	chr4:76958120-76958270	AoAF	blood vessel:	n/a	n/a
28	CTCF	chr4:76958197-76958224	LNCaP	prostate:	n/a	n/a
29	CTCF	chr4:76958184-76958204	GM19240	blood:	n/a	n/a
30	CTCF	chr4:76958149-76958246	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:76958081-76958249	HepG2	liver:	n/a	n/a
32	CUX1	chr4:76949515-76949725	K562	blood:	n/a	n/a
33	ELK1	chr4:76949655-76949735	K562	blood:	n/a	n/a
34	EP300	chr4:76958133-76958152	K562	blood:	n/a	n/a
35	EP300	chr4:76951788-76951920	K562	blood:	n/a	n/a
36	EP300	chr4:76952741-76952940	K562	blood:	n/a	chr4:76952862-76952871 chr4:76952842-76952849
37	FOS	chr4:76963404-76963774	MCF10A-Er-Src	breast:	n/a	chr4:76963583-76963593 chr4:76963582-76963593 chr4:76963582-76963594 chr4:76963583-76963592 chr4:76963584-76963591 chr4:76963583-76963593 chr4:76963584-76963593
38	FOS	chr4:76956430-76956615	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:76957055-76957501	HUVEC	blood vessel:	n/a	chr4:76957301-76957312 chr4:76957303-76957311 chr4:76957304-76957311
40	FOS	chr4:76963405-76963717	HUVEC	blood vessel:	n/a	chr4:76963583-76963593 chr4:76963582-76963593 chr4:76963582-76963594 chr4:76963583-76963592 chr4:76963584-76963591 chr4:76963583-76963593 chr4:76963584-76963593
41	FOS	chr4:76956326-76956664	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr4:76963420-76963749	MCF10A-Er-Src	breast:	n/a	chr4:76963583-76963593 chr4:76963582-76963593 chr4:76963582-76963594 chr4:76963583-76963592 chr4:76963584-76963591 chr4:76963583-76963593 chr4:76963584-76963593
43	FOS	chr4:76956245-76956587	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr4:76957049-76957459	MCF10A-Er-Src	breast:	n/a	chr4:76957301-76957312 chr4:76957303-76957311 chr4:76957304-76957311
45	FOS	chr4:76963419-76963766	MCF10A-Er-Src	breast:	n/a	chr4:76963583-76963593 chr4:76963582-76963593 chr4:76963582-76963594 chr4:76963583-76963592 chr4:76963584-76963591 chr4:76963583-76963593 chr4:76963584-76963593
46	FOS	chr4:76957108-76957481	MCF10A-Er-Src	breast:	n/a	chr4:76957301-76957312 chr4:76957303-76957311 chr4:76957304-76957311
47	FOS	chr4:76957033-76957494	MCF10A-Er-Src	breast:	n/a	chr4:76957301-76957312 chr4:76957303-76957311 chr4:76957041-76957050 chr4:76957304-76957311
48	FOS	chr4:76957173-76957442	MCF10A-Er-Src	breast:	n/a	chr4:76957301-76957312 chr4:76957303-76957311 chr4:76957304-76957311
49	FOS	chr4:76963420-76963759	MCF10A-Er-Src	breast:	n/a	chr4:76963583-76963593 chr4:76963582-76963593 chr4:76963582-76963594 chr4:76963583-76963592 chr4:76963584-76963591 chr4:76963583-76963593 chr4:76963584-76963593
50	FOSL1	chr4:76970289-76970548	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:76971098-76971148	HMEC	breast:	n/a
2	chr4:76971098-76971148	HMEC	breast:	n/a
3	chr4:76958126-76958176	PANC-1	pancreas:	n/a
4	chr4:76958054-76958104	MCF-7	breast:	n/a
5	chr4:76970912-76970962	K562	blood:	n/a
6	chr4:76970912-76970962	SK-N-MC	brain:	n/a
7	chr4:76971098-76971148	NH-A	brain:	n/a
8	chr4:76958061-76958111	LNCaP	prostate:	n/a
9	chr4:76970912-76970962	NHBE	bronchial:	n/a
10	chr4:76958054-76958104	AG04449	skin:	fetal
11	chr4:76958061-76958111	HPAEpiC	pulmonary alveolar:	n/a
12	chr4:76971098-76971148	AG09319	gingival:	n/a
13	chr4:76958054-76958104	AG04450	lung:	fetal
14	chr4:76958054-76958104	HNPCEpiC	eye:	n/a
15	chr4:76958054-76958104	HPAEpiC	pulmonary alveolar:	n/a
16	chr4:76958126-76958176	U87	brain:	n/a
17	chr4:76970912-76970962	PFSK-1	brain:	n/a
18	chr4:76958061-76958111	NH-A	brain:	n/a
19	chr4:76958061-76958111	ECC-1	luminal epithelium:	n/a
20	chr4:76958054-76958104	SK-N-SH	brain:	n/a
21	chr4:76958061-76958111	K562	blood:	n/a
22	chr4:76958061-76958111	AG09309	skin:	n/a
23	chr4:76958054-76958104	AoSMC	blood vessel:	n/a
24	chr4:76958061-76958111	HEEpiC	esophagus:	n/a
25	chr4:76958061-76958111	ProgFib	skin:	n/a
26	chr4:76971098-76971148	Hepatocyte	liver:	n/a
27	chr4:76970912-76970962	RPTEC	kidney:	n/a
28	chr4:76958061-76958111	PFSK-1	brain:	n/a
29	chr4:76958054-76958104	Hepatocyte	liver:	n/a
30	chr4:76958126-76958176	Jurkat	blood:	n/a
31	chr4:76958054-76958104	SAEC	small airway:	n/a
32	chr4:76958126-76958176	NHBE	bronchial:	n/a
33	chr4:76970912-76970962	HCT-116	colon:	n/a
34	chr4:76958061-76958111	HCF	heart:	n/a
35	chr4:76971098-76971148	Caco-2	colon:	n/a
36	chr4:76971098-76971148	HL-60	blood:	n/a
37	chr4:76970912-76970962	HRPEpiC	eye:	n/a
38	chr4:76971098-76971148	NB4	blood:	n/a
39	chr4:76958126-76958176	SKMC	muscle:	n/a
40	chr4:76970912-76970962	GM06990	blood:	n/a
41	chr4:76970912-76970962	AoSMC	blood vessel:	n/a
42	chr4:76958061-76958111	SK-N-MC	brain:	n/a
43	chr4:76970912-76970962	AG04450	lung:	fetal
44	chr4:76958054-76958104	MCF10A-Er-Src	breast:	n/a
45	chr4:76971098-76971148	NHDF-neo	bronchial:	n/a
46	chr4:76971098-76971148	HRCEpiC	kidney:	n/a
47	chr4:76958126-76958176	GM06990	blood:	n/a
48	chr4:76958054-76958104	AG10803	skin:	n/a
49	chr4:76958054-76958104	NHDF-neo	bronchial:	n/a
50	chr4:76958054-76958104	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:76956748..76960411-chr4:76960413..76963338,4	K562	blood:
2	chr4:76944817..76946865-chr4:76946950..76949448,2	MCF-7	breast:
3	chr4:76951051..76953241-chr4:76957687..76959278,2	K562	blood:
4	chr4:76950183..76953178-chr4:76959334..76961500,2	K562	blood:
5	chr4:76961032..76963158-chr4:77027696..77030643,2	K562	blood:
6	chr4:76956748..76960411-chr4:76960413..76963338,4	K562	blood:
7	chr4:76965007..76966761-chr4:77015642..77017925,2	K562	blood:
8	chr4:76946217..76947878-chr4:76952883..76955086,2	K562	blood:
9	chr4:76884899..76887580-chr4:76953090..76955387,2	K562	blood:
10	chr4:76950183..76953178-chr4:76959334..76961500,2	K562	blood:
11	chr4:76952586..76954582-chr4:76957355..76959268,3	K562	blood:
12	chr4:76932434..76934325-chr4:76957722..76960530,2	K562	blood:
13	chr4:76911559..76914179-chr4:76954597..76956782,2	MCF-7	breast:
14	chr4:76946437..76948310-chr4:76949313..76951131,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM47E-1	chr4:76965316-76965818	l_2670_chr4:76963126-76965818_testes
2	lnc-FAM47E-1	chr4:76963127-76963257	l_2670_chr4:76963126-76965818_testes

Variant related genes	Relation type
ENSG00000225846	TF binding region
CXCL10	TF binding region
CXCL11	TF binding region
ENSG00000225846	CpG island
CXCL10	CpG island
CXCL11	CpG island
ENSG00000265931	chromatin interactions
ENSG00000198301	chromatin interactions
ENSG00000156219	chromatin interactions
ENSG00000169248	chromatin interactions
ENSG00000225846	chromatin interactions

Extended variants
information (count: 1077 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1077 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369011048	chr4:76948821-76948822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535876036	chr4:76948830-76948831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369225957	chr4:76948872-76948873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148317643	chr4:76948881-76948882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189557637	chr4:76948942-76948943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574298242	chr4:76948999-76949000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs180839397	chr4:76949003-76949004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553184473	chr4:76949022-76949023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12500868	chr4:76949059-76949060	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs369793426	chr4:76949073-76949074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73825703	chr4:76949074-76949075	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs78347618	chr4:76949076-76949077	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
13	rs76860894	chr4:76949078-76949079	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
14	rs4859594	chr4:76949083-76949084	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs561334976	chr4:76949092-76949093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545964355	chr4:76949113-76949114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78422937	chr4:76949134-76949135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201610067	chr4:76949136-76949137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528404760	chr4:76949240-76949241	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs144235332	chr4:76949260-76949261	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs549643977	chr4:76949282-76949283	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs6148527	chr4:76949333-76949334	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs202095170	chr4:76949336-76949337	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs200595868	chr4:76949337-76949338	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs201377662	chr4:76949338-76949339	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs373798104	chr4:76949339-76949340	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs376473191	chr4:76949340-76949341	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs150794764	chr4:76949439-76949440	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs532348938	chr4:76949471-76949472	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs542447636	chr4:76949479-76949480	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs566591893	chr4:76949539-76949540	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs373684055	chr4:76949542-76949543	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs562002340	chr4:76949664-76949665	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs569012007	chr4:76949683-76949684	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs139217278	chr4:76949730-76949731	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs368144610	chr4:76949754-76949755	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs547904539	chr4:76949783-76949784	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs189344273	chr4:76949787-76949788	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs533519235	chr4:76949866-76949867	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs577631197	chr4:76949932-76949933	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs545946203	chr4:76949953-76949954	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs571562397	chr4:76949975-76949976	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs4859414	chr4:76949997-76949998	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs557123844	chr4:76950001-76950002	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs4859595	chr4:76950062-76950063	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs77182593	chr4:76950131-76950132	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs181796820	chr4:76950182-76950183	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs573207516	chr4:76950239-76950240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540584603	chr4:76950257-76950258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185939591	chr4:76950272-76950273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Breast cancer	21364760	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76944800-76949200	Weak transcription	Fetal Lung	lung
2	chr4:76944800-76949600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr4:76945000-76949200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:76945200-76949600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr4:76945400-76949200	Weak transcription	Adipose Nuclei	Adipose
6	chr4:76945400-76949200	Weak transcription	Liver	Liver
7	chr4:76945400-76949600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr4:76945600-76949200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr4:76945600-76949600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr4:76945800-76949200	Weak transcription	Primary B cells from peripheral blood	blood
11	chr4:76945800-76949200	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr4:76945800-76949400	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr4:76945800-76949600	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr4:76946000-76949600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr4:76946200-76949200	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr4:76946200-76949200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr4:76946400-76949200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr4:76946400-76949400	Weak transcription	Primary hematopoietic stem cells	blood
19	chr4:76949200-76949400	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr4:76949200-76949400	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr4:76949200-76949400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr4:76949200-76949400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:76949200-76949400	Enhancers	Adipose Nuclei	Adipose
24	chr4:76949200-76949400	Flanking Active TSS	Liver	Liver
25	chr4:76949200-76949400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr4:76949200-76949400	Flanking Active TSS	Fetal Lung	lung
27	chr4:76949200-76949600	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr4:76949200-76949600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
29	chr4:76949200-76949600	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr4:76949200-76949600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr4:76949200-76949600	Active TSS	Duodenum Mucosa	Duodenum
32	chr4:76949200-76949600	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr4:76949200-76949800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr4:76949200-76949800	Active TSS	Rectal Mucosa Donor 29	rectum
35	chr4:76949200-76950000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr4:76949200-76950000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr4:76949200-76950000	Active TSS	Stomach Smooth Muscle	stomach
38	chr4:76949200-76950000	Flanking Active TSS	HUVEC	blood vessel
39	chr4:76949200-76950200	Enhancers	Primary B cells from peripheral blood	blood
40	chr4:76949200-76950200	Active TSS	Duodenum Smooth Muscle	Duodenum
41	chr4:76949400-76949600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr4:76949400-76949600	Active TSS	Primary T cells from cord blood	blood
43	chr4:76949400-76949600	Enhancers	Primary hematopoietic stem cells	blood
44	chr4:76949400-76949600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr4:76949400-76949600	Active TSS	Liver	Liver
46	chr4:76949400-76949600	Enhancers	Brain Angular Gyrus	brain
47	chr4:76949400-76949600	Active TSS	Brain Substantia Nigra	brain
48	chr4:76949400-76949600	Active TSS	Fetal Stomach	stomach
49	chr4:76949400-76949600	Active TSS	Rectal Smooth Muscle	rectum
50	chr4:76949400-76949600	Flanking Active TSS	HMEC	breast

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