Variant report

Variant	nsv1001852
Chromosome Location	chr4:78135874-78260269
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:809)
CpG islands
(count:61)
Chromatin interactive
region (count:41)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:809 , 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	chr4:78169965-78170247	HepG2	liver:	n/a	n/a
4	BHLHE40	chr4:78161829-78161910	GM12878	blood:	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	chr4:78161727-78161966	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr4:78230084-78230356	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr4:78142599-78142677	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr4:78253883-78254139	K562	blood:	n/a	n/a
11	CBX3	chr4:78253824-78254202	K562	blood:	n/a	n/a
12	CBX3	chr4:78253746-78254319	HCT-116	colon:	n/a	n/a
13	CEBPB	chr4:78136969-78137231	HepG2	liver:	n/a	chr4:78137093-78137104
14	CEBPB	chr4:78215400-78215689	HepG2	liver:	n/a	chr4:78215544-78215555
15	CEBPB	chr4:78215423-78215638	IMR90	lung:	n/a	chr4:78215544-78215555
16	CEBPB	chr4:78171884-78171912	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:78227010-78227248	Hela-S3	cervix:	n/a	chr4:78227117-78227130 chr4:78227117-78227128 chr4:78227118-78227129 chr4:78227117-78227130
18	CEBPB	chr4:78226915-78227276	MCF-7	breast:	n/a	chr4:78227117-78227130 chr4:78227117-78227128 chr4:78227118-78227129 chr4:78227117-78227130
19	CEBPB	chr4:78215392-78215580	K562	blood:	n/a	chr4:78215544-78215555
20	CEBPB	chr4:78226971-78227260	K562	blood:	n/a	chr4:78227117-78227130 chr4:78227117-78227128 chr4:78227118-78227129 chr4:78227117-78227130
21	CEBPB	chr4:78226987-78227290	HepG2	liver:	n/a	chr4:78227117-78227130 chr4:78227117-78227128 chr4:78227118-78227129 chr4:78227117-78227130
22	CEBPB	chr4:78142460-78142826	IMR90	lung:	n/a	n/a
23	CEBPB	chr4:78136939-78137228	A549	lung:	n/a	chr4:78137093-78137104
24	CEBPB	chr4:78142464-78142815	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr4:78169257-78169440	HepG2	liver:	n/a	n/a
26	CHD2	chr4:78230108-78230195	HepG2	liver:	n/a	n/a
27	CHD2	chr4:78254095-78254505	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr4:78230080-78230324	HepG2	liver:	n/a	n/a
29	CTCF	chr4:78227000-78227150	HMF	breast:	n/a	chr4:78227096-78227117 chr4:78227101-78227119 chr4:78227103-78227116
30	CTCF	chr4:78230100-78230250	BE2_C	brain:	n/a	n/a
31	CTCF	chr4:78230160-78230310	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:78161720-78161870	NHEK	skin:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
33	CTCF	chr4:78230078-78230338	GM12878	blood:	n/a	n/a
34	CTCF	chr4:78230160-78230310	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr4:78173055-78173102	GM20000	blood:	n/a	n/a
36	CTCF	chr4:78161519-78161554	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr4:78161740-78161890	GM12875	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
38	CTCF	chr4:78230100-78230250	RPTEC	kidney:	n/a	n/a
39	CTCF	chr4:78230134-78230256	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr4:78197240-78197390	GM12872	blood:	n/a	n/a
41	CTCF	chr4:78230029-78230389	IMR90	lung:	n/a	n/a
42	CTCF	chr4:78161060-78161210	AG10803	skin:	n/a	n/a
43	CTCF	chr4:78227000-78227150	SAEC	small airway:	n/a	chr4:78227096-78227117 chr4:78227101-78227119 chr4:78227103-78227116
44	CTCF	chr4:78170674-78170739	LNCaP	prostate:	n/a	chr4:78170675-78170684
45	CTCF	chr4:78230580-78230730	HCM	heart:	n/a	n/a
46	CTCF	chr4:78161626-78161989	T-47D	breast:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
47	CTCF	chr4:78161740-78161890	MCF-7	breast:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
48	CTCF	chr4:78161740-78161890	HMF	breast:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
49	CTCF	chr4:78161692-78161944	Kidney_OC	kidney:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
50	CTCF	chr4:78197286-78197491	K562	blood:	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	NT2-D1	testis:	n/a
2	chr4:78156196-78156246	NHDF-neo	bronchial:	n/a
3	chr4:78156196-78156246	HCPEpiC	choroid plexus:	n/a
4	chr4:78156196-78156246	ProgFib	skin:	n/a
5	chr4:78156196-78156246	AG04450	lung:	fetal
6	chr4:78156196-78156246	PFSK-1	brain:	n/a
7	chr4:78156196-78156246	AG10803	skin:	n/a
8	chr4:78156196-78156246	SK-N-SH_RA	brain:	n/a
9	chr4:78156196-78156246	Caco-2	colon:	n/a
10	chr4:78156196-78156246	MCF-7	breast:	n/a
11	chr4:78156196-78156246	ECC-1	luminal epithelium:	n/a
12	chr4:78156196-78156246	PrEC	prostate:	n/a
13	chr4:78156196-78156246	GM06990	blood:	n/a
14	chr4:78156196-78156246	T-47D	breast:	n/a
15	chr4:78156196-78156246	SKMC	muscle:	n/a
16	chr4:78156196-78156246	RPTEC	kidney:	n/a
17	chr4:78156196-78156246	H1-hESC	embryonic stem cell:	embryo
18	chr4:78156196-78156246	BE2_C	brain:	n/a
19	chr4:78156196-78156246	HEK293	kidney:	embryo
20	chr4:78156196-78156246	AoSMC	blood vessel:	n/a
21	chr4:78156196-78156246	SK-N-SH	brain:	n/a
22	chr4:78156196-78156246	HCM	heart:	n/a
23	chr4:78156196-78156246	LNCaP	prostate:	n/a
24	chr4:78156196-78156246	HNPCEpiC	eye:	n/a
25	chr4:78156196-78156246	HepG2	liver:	n/a
26	chr4:78156196-78156246	GM12892	blood:	n/a
27	chr4:78156196-78156246	AG09309	skin:	n/a
28	chr4:78156196-78156246	ovcar-3	ovarian:	n/a
29	chr4:78156196-78156246	HMEC	breast:	n/a
30	chr4:78156196-78156246	MCF10A-Er-Src	breast:	n/a
31	chr4:78156196-78156246	Hepatocyte	liver:	n/a
32	chr4:78156196-78156246	NH-A	brain:	n/a
33	chr4:78156196-78156246	AG04449	skin:	fetal
34	chr4:78156196-78156246	GM12878	blood:	n/a
35	chr4:78156196-78156246	SAEC	small airway:	n/a
36	chr4:78156196-78156246	GM19239	blood:	n/a
37	chr4:78156196-78156246	Jurkat	blood:	n/a
38	chr4:78156196-78156246	HRCEpiC	kidney:	n/a
39	chr4:78156196-78156246	Hela-S3	cervix:	n/a
40	chr4:78156196-78156246	HAEpiC	amniotic membrane:	n/a
41	chr4:78156196-78156246	K562	blood:	n/a
42	chr4:78156196-78156246	IMR90	lung:	fetal
43	chr4:78156196-78156246	HCT-116	colon:	n/a
44	chr4:78156196-78156246	HUVEC	blood vessel:	n/a
45	chr4:78156196-78156246	CMK	blood:	n/a
46	chr4:78156196-78156246	U87	brain:	n/a
47	chr4:78156196-78156246	HEEpiC	esophagus:	n/a
48	chr4:78156196-78156246	HPAEpiC	pulmonary alveolar:	n/a
49	chr4:78156196-78156246	GM12891	blood:	n/a
50	chr4:78156196-78156246	BJ	skin:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:78257188..78259774-chr4:78266144..78268332,2	K562	blood:
2	chr4:77994973..77997901-chr4:78150275..78153619,3	MCF-7	breast:
3	chr4:78182930..78185790-chr4:78187841..78189605,2	K562	blood:
4	chr4:78155252..78157365-chr4:78224145..78227144,3	MCF-7	breast:
5	chr4:78155252..78157365-chr4:78224145..78227144,3	MCF-7	breast:
6	chr4:78161284..78162458-chr4:78229777..78230742,7	K562	blood:
7	chr4:78149304..78151645-chr4:78154973..78157716,3	K562	blood:
8	chr4:78182930..78185790-chr4:78187841..78189605,2	K562	blood:
9	chr4:78016448..78019261-chr4:78148834..78151500,2	MCF-7	breast:
10	chr4:78161188..78162532-chr4:78229476..78230856,15	MCF-7	breast:
11	chr4:78236163..78238480-chr4:78287943..78289669,2	K562	blood:
12	chr4:78229797..78230625-chr4:78279333..78280102,3	MCF-7	breast:
13	chr4:78149304..78151645-chr4:78154973..78157716,3	K562	blood:
14	chr4:78162165..78163774-chr4:78227168..78228953,2	MCF-7	breast:
15	chr4:78130169..78132632-chr4:78133437..78136630,3	K562	blood:
16	chr4:78161721..78162270-chr4:78279119..78279681,2	MCF-7	breast:
17	chr4:78161284..78162458-chr4:78229777..78230742,7	K562	blood:
18	chr4:78230184..78230702-chr4:78278364..78278865,2	MCF-7	breast:
19	chr4:78174499..78176837-chr4:78205161..78207032,2	MCF-7	breast:
20	chr4:78155142..78157870-chr4:78168469..78170209,2	MCF-7	breast:
21	chr4:77973179..77974099-chr4:78229775..78230650,3	K562	blood:
22	chr4:78161188..78162532-chr4:78229476..78230856,15	MCF-7	breast:
23	chr4:78162165..78163774-chr4:78227168..78228953,2	MCF-7	breast:
24	chr4:78155142..78157870-chr4:78168469..78170209,2	MCF-7	breast:
25	chr4:78161416..78162110-chr4:78226527..78227315,3	MCF-7	breast:
26	chr4:78174499..78176837-chr4:78205161..78207032,2	MCF-7	breast:
27	chr4:78132153..78134677-chr4:78134780..78136645,2	MCF-7	breast:
28	chr4:78177354..78179710-chr4:78180664..78183643,2	MCF-7	breast:
29	chr4:78158067..78160012-chr4:78227264..78228770,2	MCF-7	breast:
30	chr4:78161311..78162711-chr4:78226629..78227614,14	MCF-7	breast:
31	chr4:78160754..78162321-chr4:78226906..78228617,2	MCF-7	breast:
32	chr4:78161398..78162211-chr4:78229720..78230660,3	MCF-7	breast:
33	chr4:78161311..78162711-chr4:78226629..78227614,14	MCF-7	breast:
34	chr4:78177354..78179710-chr4:78180664..78183643,2	MCF-7	breast:
35	chr4:78161365..78162334-chr4:78279195..78280134,7	K562	blood:
36	chr4:78161398..78162211-chr4:78229720..78230660,3	MCF-7	breast:
37	chr4:78161324..78162321-chr4:78279149..78280134,4	MCF-7	breast:
38	chr4:78161416..78162110-chr4:78226527..78227315,3	MCF-7	breast:
39	chr4:78160754..78162321-chr4:78226906..78228617,2	MCF-7	breast:
40	chr4:78161473..78162127-chr4:78394685..78395318,2	K562	blood:
41	chr4:78158067..78160012-chr4:78227264..78228770,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCNI-5	chr4:78232550-78233264	NONHSAT097052
2	lnc-CCNI-4	chr4:78137569-78138031	NONHSAT097051

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: 5762 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:5762 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10028268	chr4:78135874-78135875	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191394979	chr4:78135891-78135892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78964370	chr4:78135909-78135910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76249849	chr4:78135910-78135911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79688349	chr4:78135911-78135912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542696974	chr4:78135941-78135942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559461902	chr4:78135970-78135971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149416464	chr4:78135973-78135974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551760445	chr4:78135979-78135980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571813895	chr4:78135985-78135986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531258328	chr4:78135988-78135989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551016330	chr4:78136019-78136020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567830231	chr4:78136024-78136025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535113179	chr4:78136101-78136102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536886098	chr4:78136194-78136195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79237891	chr4:78136199-78136200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148536201	chr4:78136219-78136220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183922022	chr4:78136242-78136243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557751650	chr4:78136249-78136250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6817538	chr4:78136251-78136252	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs188632011	chr4:78136273-78136274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142757949	chr4:78136299-78136300	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573494067	chr4:78136327-78136328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs61315482	chr4:78136395-78136396	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs559378455	chr4:78136425-78136426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528576468	chr4:78136469-78136470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545043265	chr4:78136481-78136482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1862361	chr4:78136519-78136520	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs191892702	chr4:78136530-78136531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147672595	chr4:78136535-78136536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568005901	chr4:78136564-78136565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185205017	chr4:78136597-78136598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547226185	chr4:78136660-78136661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372365244	chr4:78136670-78136671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565746614	chr4:78136682-78136683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113951517	chr4:78136685-78136686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534729495	chr4:78136705-78136706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534878076	chr4:78136734-78136735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372960071	chr4:78136751-78136752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571209482	chr4:78136753-78136754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs17002445	chr4:78136776-78136777	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs57714876	chr4:78136777-78136778	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs573605639	chr4:78136792-78136793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536005687	chr4:78136804-78136805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376902459	chr4:78136832-78136833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140738875	chr4:78136839-78136840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145286956	chr4:78136866-78136867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190395640	chr4:78136887-78136888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147652819	chr4:78136893-78136894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11937061	chr4:78136933-78136934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease

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:209 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78125200-78143600	Weak transcription	Primary B cells from cord blood	blood
2	chr4:78136200-78136800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:78136400-78136600	Enhancers	Fetal Heart	heart
4	chr4:78136400-78136800	Enhancers	Fetal Muscle Leg	muscle
5	chr4:78136600-78139600	Weak transcription	Fetal Heart	heart
6	chr4:78136800-78139200	Weak transcription	Fetal Muscle Leg	muscle
7	chr4:78139200-78140600	Enhancers	Fetal Muscle Leg	muscle
8	chr4:78139600-78140000	Enhancers	Fetal Heart	heart
9	chr4:78140000-78140200	Weak transcription	Fetal Heart	heart
10	chr4:78140200-78144000	Enhancers	Fetal Heart	heart
11	chr4:78140600-78141800	Weak transcription	Fetal Muscle Leg	muscle
12	chr4:78141800-78142800	Enhancers	Fetal Muscle Leg	muscle
13	chr4:78141800-78143200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:78142000-78143000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr4:78142000-78143000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:78142200-78142400	Enhancers	Aorta	Aorta
17	chr4:78142200-78142800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr4:78142200-78142800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr4:78142200-78143200	Bivalent Enhancer	Osteobl	bone
20	chr4:78142400-78142600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr4:78142600-78143200	Enhancers	Fetal Lung	lung
22	chr4:78142800-78145600	Weak transcription	Fetal Muscle Leg	muscle
23	chr4:78143200-78143400	Enhancers	Aorta	Aorta
24	chr4:78143200-78143400	Enhancers	Fetal Muscle Trunk	muscle
25	chr4:78145600-78147200	Enhancers	Fetal Muscle Leg	muscle
26	chr4:78146000-78146200	Enhancers	Fetal Muscle Trunk	muscle
27	chr4:78146000-78146600	Enhancers	Right Atrium	heart
28	chr4:78146000-78147400	Enhancers	Fetal Heart	heart
29	chr4:78146200-78147800	Weak transcription	Fetal Muscle Trunk	muscle
30	chr4:78147400-78152200	Weak transcription	Fetal Heart	heart
31	chr4:78147600-78148000	Weak transcription	Primary B cells from cord blood	blood
32	chr4:78147800-78148800	ZNF genes & repeats	Fetal Muscle Trunk	muscle
33	chr4:78148000-78149000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr4:78148600-78148800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr4:78148600-78148800	Enhancers	HMEC	breast
36	chr4:78148800-78153600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr4:78149000-78156400	Weak transcription	Primary B cells from cord blood	blood
38	chr4:78149200-78150400	Weak transcription	HMEC	breast
39	chr4:78150000-78150800	Enhancers	Esophagus	oesophagus
40	chr4:78150000-78151000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr4:78150400-78151200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr4:78150400-78151200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:78150400-78151400	Enhancers	HMEC	breast
44	chr4:78150400-78151400	Enhancers	NHEK	skin
45	chr4:78150800-78153400	Weak transcription	Esophagus	oesophagus
46	chr4:78151200-78153600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:78152200-78153400	Enhancers	Fetal Heart	heart
48	chr4:78152400-78156000	Weak transcription	Primary T cells from cord blood	blood
49	chr4:78153400-78153800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr4:78153400-78153800	Enhancers	Esophagus	oesophagus

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