Variant report

Variant	nsv1010406
Chromosome Location	chr4:78139780-78255427
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:801)
CpG islands
(count:61)
Chromatin interactive
region (count:38)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:801 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

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	chr4:78230084-78230356	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr4:78161727-78161966	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr4:78142599-78142677	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr4:78161761-78161808	GM12878	blood:	n/a	n/a
10	CBX3	chr4:78253746-78254319	HCT-116	colon:	n/a	n/a
11	CBX3	chr4:78253824-78254202	K562	blood:	n/a	n/a
12	CBX3	chr4:78253883-78254139	K562	blood:	n/a	n/a
13	CEBPB	chr4:78226987-78227290	HepG2	liver:	n/a	chr4:78227117-78227130 chr4:78227117-78227128 chr4:78227118-78227129 chr4:78227117-78227130
14	CEBPB	chr4:78226915-78227276	MCF-7	breast:	n/a	chr4:78227117-78227130 chr4:78227117-78227128 chr4:78227118-78227129 chr4:78227117-78227130
15	CEBPB	chr4:78169257-78169440	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:78142460-78142826	IMR90	lung:	n/a	n/a
17	CEBPB	chr4:78215392-78215580	K562	blood:	n/a	chr4:78215544-78215555
18	CEBPB	chr4:78142464-78142815	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr4:78171884-78171912	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:78215400-78215689	HepG2	liver:	n/a	chr4:78215544-78215555
21	CEBPB	chr4:78227010-78227248	Hela-S3	cervix:	n/a	chr4:78227117-78227130 chr4:78227117-78227128 chr4:78227118-78227129 chr4:78227117-78227130
22	CEBPB	chr4:78215423-78215638	IMR90	lung:	n/a	chr4:78215544-78215555
23	CEBPB	chr4:78226971-78227260	K562	blood:	n/a	chr4:78227117-78227130 chr4:78227117-78227128 chr4:78227118-78227129 chr4:78227117-78227130
24	CHD2	chr4:78230108-78230195	HepG2	liver:	n/a	n/a
25	CHD2	chr4:78254095-78254505	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr4:78230120-78230270	HL-60	blood:	n/a	n/a
27	CTCF	chr4:78230077-78230342	HUVEC	blood vessel:	n/a	n/a
28	CTCF	chr4:78230160-78230310	A549	lung:	n/a	n/a
29	CTCF	chr4:78161760-78161928	A549	lung:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
30	CTCF	chr4:78161325-78162253	SK-N-SH	brain:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
31	CTCF	chr4:78230160-78230310	AG09309	skin:	n/a	n/a
32	CTCF	chr4:78230060-78230210	WI-38	lung:	n/a	n/a
33	CTCF	chr4:78161740-78161890	HRE	kidney:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
34	CTCF	chr4:78170680-78170830	HPF	lung:	n/a	n/a
35	CTCF	chr4:78230140-78230290	AG09319	gingival:	n/a	n/a
36	CTCF	chr4:78230180-78230330	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr4:78161700-78161850	HCT-116	colon:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
38	CTCF	chr4:78230120-78230270	GM12868	blood:	n/a	n/a
39	CTCF	chr4:78230160-78230310	HCFaa	heart:	n/a	n/a
40	CTCF	chr4:78161667-78161967	K562	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
41	CTCF	chr4:78198780-78198930	GM12868	blood:	n/a	n/a
42	CTCF	chr4:78229999-78230289	A549	lung:	n/a	n/a
43	CTCF	chr4:78161692-78161944	Kidney_OC	kidney:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
44	CTCF	chr4:78161740-78161890	HUVEC	blood vessel:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
45	CTCF	chr4:78161760-78161910	AG09319	gingival:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
46	CTCF	chr4:78161720-78161870	NHEK	skin:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
47	CTCF	chr4:78161740-78161890	GM06990	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
48	CTCF	chr4:78161720-78161870	AG09309	skin:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
49	CTCF	chr4:78162180-78162330	GM12868	blood:	n/a	n/a
50	CTCF	chr4:78170680-78170830	HRPEpiC	eye:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78156196-78156246	HL-60	blood:	n/a
2	chr4:78156196-78156246	NHBE	bronchial:	n/a
3	chr4:78156196-78156246	HCT-116	colon:	n/a
4	chr4:78156196-78156246	AG09319	gingival:	n/a
5	chr4:78156196-78156246	AG10803	skin:	n/a
6	chr4:78156196-78156246	AG09309	skin:	n/a
7	chr4:78156196-78156246	GM12891	blood:	n/a
8	chr4:78156196-78156246	MCF10A-Er-Src	breast:	n/a
9	chr4:78156196-78156246	AG04450	lung:	fetal
10	chr4:78156196-78156246	SK-N-MC	brain:	n/a
11	chr4:78156196-78156246	HepG2	liver:	n/a
12	chr4:78156196-78156246	HRPEpiC	eye:	n/a
13	chr4:78156196-78156246	PFSK-1	brain:	n/a
14	chr4:78156196-78156246	Hepatocyte	liver:	n/a
15	chr4:78156196-78156246	ECC-1	luminal epithelium:	n/a
16	chr4:78156196-78156246	BE2_C	brain:	n/a
17	chr4:78156196-78156246	SAEC	small airway:	n/a
18	chr4:78156196-78156246	NHDF-neo	bronchial:	n/a
19	chr4:78156196-78156246	SK-N-SH	brain:	n/a
20	chr4:78156196-78156246	NB4	blood:	n/a
21	chr4:78156196-78156246	GM12878	blood:	n/a
22	chr4:78156196-78156246	HIPEpiC	eye:	n/a
23	chr4:78156196-78156246	PrEC	prostate:	n/a
24	chr4:78156196-78156246	GM12892	blood:	n/a
25	chr4:78156196-78156246	BJ	skin:	n/a
26	chr4:78156196-78156246	H1-hESC	embryonic stem cell:	embryo
27	chr4:78156196-78156246	HNPCEpiC	eye:	n/a
28	chr4:78156196-78156246	HMEC	breast:	n/a
29	chr4:78156196-78156246	Caco-2	colon:	n/a
30	chr4:78156196-78156246	HCM	heart:	n/a
31	chr4:78156196-78156246	HAEpiC	amniotic membrane:	n/a
32	chr4:78156196-78156246	Hela-S3	cervix:	n/a
33	chr4:78156196-78156246	K562	blood:	n/a
34	chr4:78156196-78156246	Jurkat	blood:	n/a
35	chr4:78156196-78156246	HRCEpiC	kidney:	n/a
36	chr4:78156196-78156246	HEK293	kidney:	embryo
37	chr4:78156196-78156246	HUVEC	blood vessel:	n/a
38	chr4:78156196-78156246	NH-A	brain:	n/a
39	chr4:78156196-78156246	LNCaP	prostate:	n/a
40	chr4:78156196-78156246	RPTEC	kidney:	n/a
41	chr4:78156196-78156246	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:78156196-78156246	ProgFib	skin:	n/a
43	chr4:78156196-78156246	IMR90	lung:	fetal
44	chr4:78156196-78156246	CMK	blood:	n/a
45	chr4:78156196-78156246	ovcar-3	ovarian:	n/a
46	chr4:78156196-78156246	PANC-1	pancreas:	n/a
47	chr4:78156196-78156246	MCF-7	breast:	n/a
48	chr4:78156196-78156246	U87	brain:	n/a
49	chr4:78156196-78156246	NT2-D1	testis:	n/a
50	chr4:78156196-78156246	GM19239	blood:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:78229797..78230625-chr4:78279333..78280102,3	MCF-7	breast:
2	chr4:78174499..78176837-chr4:78205161..78207032,2	MCF-7	breast:
3	chr4:78161324..78162321-chr4:78279149..78280134,4	MCF-7	breast:
4	chr4:78161311..78162711-chr4:78226629..78227614,14	MCF-7	breast:
5	chr4:78161188..78162532-chr4:78229476..78230856,15	MCF-7	breast:
6	chr4:78155252..78157365-chr4:78224145..78227144,3	MCF-7	breast:
7	chr4:78155142..78157870-chr4:78168469..78170209,2	MCF-7	breast:
8	chr4:78158067..78160012-chr4:78227264..78228770,2	MCF-7	breast:
9	chr4:78161365..78162334-chr4:78279195..78280134,7	K562	blood:
10	chr4:78160754..78162321-chr4:78226906..78228617,2	MCF-7	breast:
11	chr4:78162165..78163774-chr4:78227168..78228953,2	MCF-7	breast:
12	chr4:78177354..78179710-chr4:78180664..78183643,2	MCF-7	breast:
13	chr4:78174499..78176837-chr4:78205161..78207032,2	MCF-7	breast:
14	chr4:78182930..78185790-chr4:78187841..78189605,2	K562	blood:
15	chr4:78161398..78162211-chr4:78229720..78230660,3	MCF-7	breast:
16	chr4:78161398..78162211-chr4:78229720..78230660,3	MCF-7	breast:
17	chr4:78149304..78151645-chr4:78154973..78157716,3	K562	blood:
18	chr4:78158067..78160012-chr4:78227264..78228770,2	MCF-7	breast:
19	chr4:78161284..78162458-chr4:78229777..78230742,7	K562	blood:
20	chr4:78161188..78162532-chr4:78229476..78230856,15	MCF-7	breast:
21	chr4:78177354..78179710-chr4:78180664..78183643,2	MCF-7	breast:
22	chr4:78155142..78157870-chr4:78168469..78170209,2	MCF-7	breast:
23	chr4:78182930..78185790-chr4:78187841..78189605,2	K562	blood:
24	chr4:78236163..78238480-chr4:78287943..78289669,2	K562	blood:
25	chr4:77973179..77974099-chr4:78229775..78230650,3	K562	blood:
26	chr4:78230184..78230702-chr4:78278364..78278865,2	MCF-7	breast:
27	chr4:78162165..78163774-chr4:78227168..78228953,2	MCF-7	breast:
28	chr4:77994973..77997901-chr4:78150275..78153619,3	MCF-7	breast:
29	chr4:78160754..78162321-chr4:78226906..78228617,2	MCF-7	breast:
30	chr4:78161473..78162127-chr4:78394685..78395318,2	K562	blood:
31	chr4:78161284..78162458-chr4:78229777..78230742,7	K562	blood:
32	chr4:78161311..78162711-chr4:78226629..78227614,14	MCF-7	breast:
33	chr4:78161721..78162270-chr4:78279119..78279681,2	MCF-7	breast:
34	chr4:78155252..78157365-chr4:78224145..78227144,3	MCF-7	breast:
35	chr4:78161416..78162110-chr4:78226527..78227315,3	MCF-7	breast:
36	chr4:78016448..78019261-chr4:78148834..78151500,2	MCF-7	breast:
37	chr4:78161416..78162110-chr4:78226527..78227315,3	MCF-7	breast:
38	chr4:78149304..78151645-chr4:78154973..78157716,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCNI-5	chr4:78232550-78233264	NONHSAT097052

No data

Variant related genes	Relation type
ENSG00000270669	TF binding region
ENSG00000250006	TF binding region
ENSG00000270669	CpG island
ENSG00000250006	CpG island
ENSG00000118816	chromatin interactions

Extended variants
information (count: 5349 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:5349 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6820366	chr4:78139780-78139781	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555563823	chr4:78139799-78139800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572335211	chr4:78139803-78139804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539937191	chr4:78139817-78139818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368028959	chr4:78139827-78139828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560234837	chr4:78139833-78139834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148693696	chr4:78139843-78139844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545789896	chr4:78139873-78139874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192081321	chr4:78139887-78139888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531657014	chr4:78140008-78140009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183787915	chr4:78140024-78140025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561847685	chr4:78140025-78140026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375755106	chr4:78140041-78140042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2007091	chr4:78140042-78140043	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs530648917	chr4:78140080-78140081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547568825	chr4:78140105-78140106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570926178	chr4:78140108-78140109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539409248	chr4:78140140-78140141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187894860	chr4:78140202-78140203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538003746	chr4:78140223-78140224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117975614	chr4:78140224-78140225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs200486348	chr4:78140226-78140227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371599931	chr4:78140227-78140228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191168587	chr4:78140229-78140230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572296422	chr4:78140296-78140297	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs367590675	chr4:78140319-78140320	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs553543232	chr4:78140328-78140329	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs77865176	chr4:78140344-78140345	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs572945785	chr4:78140360-78140361	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs538839372	chr4:78140369-78140370	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs78612639	chr4:78140379-78140380	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs562491880	chr4:78140395-78140396	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs116406780	chr4:78140405-78140406	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs558424332	chr4:78140441-78140442	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs542134196	chr4:78140454-78140455	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs562007008	chr4:78140464-78140465	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs527436063	chr4:78140474-78140475	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs554530315	chr4:78140551-78140552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75450238	chr4:78140600-78140601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564389165	chr4:78140612-78140613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552630770	chr4:78140625-78140626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182211512	chr4:78140628-78140629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs151201689	chr4:78140641-78140642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs72863278	chr4:78140657-78140658	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs13121366	chr4:78140669-78140670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs13121367	chr4:78140670-78140671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs13101721	chr4:78140677-78140678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs13147851	chr4:78140678-78140679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529289099	chr4:78140685-78140686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs13121380	chr4:78140694-78140695	Weak transcription Enhancers	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:193 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78125200-78143600	Weak transcription	Primary B cells from cord blood	blood
2	chr4:78139200-78140600	Enhancers	Fetal Muscle Leg	muscle
3	chr4:78139600-78140000	Enhancers	Fetal Heart	heart
4	chr4:78140000-78140200	Weak transcription	Fetal Heart	heart
5	chr4:78140200-78144000	Enhancers	Fetal Heart	heart
6	chr4:78140600-78141800	Weak transcription	Fetal Muscle Leg	muscle
7	chr4:78141800-78142800	Enhancers	Fetal Muscle Leg	muscle
8	chr4:78141800-78143200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:78142000-78143000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:78142000-78143000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:78142200-78142400	Enhancers	Aorta	Aorta
12	chr4:78142200-78142800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:78142200-78142800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr4:78142200-78143200	Bivalent Enhancer	Osteobl	bone
15	chr4:78142400-78142600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr4:78142600-78143200	Enhancers	Fetal Lung	lung
17	chr4:78142800-78145600	Weak transcription	Fetal Muscle Leg	muscle
18	chr4:78143200-78143400	Enhancers	Aorta	Aorta
19	chr4:78143200-78143400	Enhancers	Fetal Muscle Trunk	muscle
20	chr4:78145600-78147200	Enhancers	Fetal Muscle Leg	muscle
21	chr4:78146000-78146200	Enhancers	Fetal Muscle Trunk	muscle
22	chr4:78146000-78146600	Enhancers	Right Atrium	heart
23	chr4:78146000-78147400	Enhancers	Fetal Heart	heart
24	chr4:78146200-78147800	Weak transcription	Fetal Muscle Trunk	muscle
25	chr4:78147400-78152200	Weak transcription	Fetal Heart	heart
26	chr4:78147600-78148000	Weak transcription	Primary B cells from cord blood	blood
27	chr4:78147800-78148800	ZNF genes & repeats	Fetal Muscle Trunk	muscle
28	chr4:78148000-78149000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr4:78148600-78148800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:78148600-78148800	Enhancers	HMEC	breast
31	chr4:78148800-78153600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:78149000-78156400	Weak transcription	Primary B cells from cord blood	blood
33	chr4:78149200-78150400	Weak transcription	HMEC	breast
34	chr4:78150000-78150800	Enhancers	Esophagus	oesophagus
35	chr4:78150000-78151000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:78150400-78151200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:78150400-78151200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr4:78150400-78151400	Enhancers	HMEC	breast
39	chr4:78150400-78151400	Enhancers	NHEK	skin
40	chr4:78150800-78153400	Weak transcription	Esophagus	oesophagus
41	chr4:78151200-78153600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr4:78152200-78153400	Enhancers	Fetal Heart	heart
43	chr4:78152400-78156000	Weak transcription	Primary T cells from cord blood	blood
44	chr4:78153400-78153800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr4:78153400-78153800	Enhancers	Esophagus	oesophagus
46	chr4:78153400-78154600	Weak transcription	Fetal Heart	heart
47	chr4:78153600-78153800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:78153600-78153800	Enhancers	Fetal Intestine Large	intestine
49	chr4:78153600-78154400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:78154200-78154400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin

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