Variant report

Variant	nsv596441
Chromosome Location	chr4:187695564-187786316
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1229)
CpG islands
(count:734)
Chromatin interactive
region (count:76)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1229 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:187720138-187720676	K562	blood:	n/a	n/a
2	ARID3A	chr4:187773395-187773671	K562	blood:	n/a	n/a
3	ARID3A	chr4:187760277-187761324	K562	blood:	n/a	n/a
4	ARID3A	chr4:187746209-187746605	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:187759533-187759733	K562	blood:	n/a	n/a
6	ARID3A	chr4:187741826-187742105	K562	blood:	n/a	n/a
7	ARID3A	chr4:187702603-187703219	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:187729354-187730202	K562	blood:	n/a	n/a
9	ARID3A	chr4:187765085-187766847	K562	blood:	n/a	n/a
10	ARID3A	chr4:187725992-187727103	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:187745168-187745605	K562	blood:	n/a	n/a
12	ARID3A	chr4:187754097-187754356	K562	blood:	n/a	n/a
13	ARID3A	chr4:187751015-187751336	K562	blood:	n/a	n/a
14	ATF1	chr4:187720136-187720604	K562	blood:	n/a	n/a
15	ATF1	chr4:187754084-187754825	K562	blood:	n/a	n/a
16	ATF1	chr4:187766234-187766973	K562	blood:	n/a	n/a
17	ATF1	chr4:187750478-187751308	K562	blood:	n/a	n/a
18	ATF2	chr4:187741737-187742063	GM12878	blood:	n/a	n/a
19	ATF2	chr4:187774172-187774562	GM12878	blood:	n/a	n/a
20	ATF3	chr4:187765980-187766895	K562	blood:	n/a	n/a
21	ATF3	chr4:187750933-187751363	K562	blood:	n/a	n/a
22	ATF3	chr4:187766276-187766741	K562	blood:	n/a	n/a
23	ATF3	chr4:187729756-187730113	K562	blood:	n/a	n/a
24	BACH1	chr4:187729940-187730111	K562	blood:	n/a	n/a
25	BACH1	chr4:187742277-187743075	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr4:187760500-187760676	K562	blood:	n/a	n/a
27	BACH1	chr4:187773306-187773479	K562	blood:	n/a	n/a
28	BACH1	chr4:187766200-187766678	K562	blood:	n/a	chr4:187766407-187766421 chr4:187766651-187766665
29	BATF	chr4:187742315-187742944	GM12878	blood:	n/a	n/a
30	BATF	chr4:187741798-187742035	GM12878	blood:	n/a	chr4:187741973-187741983
31	BATF	chr4:187760646-187761031	GM12878	blood:	n/a	chr4:187760826-187760836 chr4:187760825-187760836 chr4:187760784-187760793
32	BATF	chr4:187773931-187774451	GM12878	blood:	n/a	chr4:187774310-187774318
33	BATF	chr4:187760733-187760988	GM12878	blood:	n/a	chr4:187760826-187760836 chr4:187760825-187760836 chr4:187760784-187760793
34	BCL11A	chr4:187741718-187742077	GM12878	blood:	n/a	chr4:187741976-187741985 chr4:187741975-187741984
35	BCL11A	chr4:187760706-187761047	GM12878	blood:	n/a	chr4:187760824-187760833 chr4:187760894-187760903 chr4:187760825-187760834
36	BCL11A	chr4:187742270-187742955	GM12878	blood:	n/a	n/a
37	BCL11A	chr4:187774188-187774596	GM12878	blood:	n/a	n/a
38	BCLAF1	chr4:187766190-187767004	K562	blood:	n/a	chr4:187766814-187766823 chr4:187766409-187766418 chr4:187766654-187766663 chr4:187766410-187766419
39	BHLHE40	chr4:187766222-187766996	K562	blood:	n/a	n/a
40	BHLHE40	chr4:187764665-187764865	K562	blood:	n/a	n/a
41	BHLHE40	chr4:187765114-187765531	K562	blood:	n/a	n/a
42	BHLHE40	chr4:187729579-187729987	K562	blood:	n/a	n/a
43	BHLHE40	chr4:187750534-187751306	K562	blood:	n/a	n/a
44	BHLHE40	chr4:187720133-187720422	K562	blood:	n/a	n/a
45	BHLHE40	chr4:187761798-187762453	K562	blood:	n/a	n/a
46	BRCA1	chr4:187750648-187751418	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr4:187765551-187765979	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr4:187766141-187767060	K562	blood:	n/a	chr4:187766312-187766323
49	CBX3	chr4:187750830-187751331	K562	blood:	n/a	n/a
50	CBX3	chr4:187742275-187743023	K562	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187761401-187761451	MCF-7	breast:	n/a
2	chr4:187783798-187783848	SK-N-SH	brain:	n/a
3	chr4:187761401-187761451	MCF-7	breast:	n/a
4	chr4:187783798-187783848	SK-N-SH	brain:	n/a
5	chr4:187765617-187765667	MCF10A-Er-Src	breast:	n/a
6	chr4:187740664-187740714	HCT-116	colon:	n/a
7	chr4:187762379-187762429	GM12892	blood:	n/a
8	chr4:187702884-187702934	HEK293	kidney:	embryo
9	chr4:187761401-187761451	HAEpiC	amniotic membrane:	n/a
10	chr4:187766591-187766641	SK-N-MC	brain:	n/a
11	chr4:187762379-187762429	HNPCEpiC	eye:	n/a
12	chr4:187729190-187729240	PANC-1	pancreas:	n/a
13	chr4:187766591-187766641	U87	brain:	n/a
14	chr4:187762312-187762362	AG04450	lung:	fetal
15	chr4:187740664-187740714	GM12892	blood:	n/a
16	chr4:187766591-187766641	HRCEpiC	kidney:	n/a
17	chr4:187783798-187783848	BE2_C	brain:	n/a
18	chr4:187776068-187776118	H1-hESC	embryonic stem cell:	embryo
19	chr4:187702884-187702934	MCF-7	breast:	n/a
20	chr4:187762256-187762306	HAEpiC	amniotic membrane:	n/a
21	chr4:187783798-187783848	MCF10A-Er-Src	breast:	n/a
22	chr4:187702884-187702934	NHBE	bronchial:	n/a
23	chr4:187702884-187702934	HUVEC	blood vessel:	n/a
24	chr4:187761401-187761451	Hepatocyte	liver:	n/a
25	chr4:187765617-187765667	SK-N-MC	brain:	n/a
26	chr4:187783798-187783848	SKMC	muscle:	n/a
27	chr4:187783798-187783848	AG09309	skin:	n/a
28	chr4:187751549-187751599	H1-hESC	embryonic stem cell:	embryo
29	chr4:187766591-187766641	HCT-116	colon:	n/a
30	chr4:187776068-187776118	AG04449	skin:	fetal
31	chr4:187740664-187740714	AG10803	skin:	n/a
32	chr4:187776068-187776118	AG09319	gingival:	n/a
33	chr4:187776068-187776118	LNCaP	prostate:	n/a
34	chr4:187776068-187776118	NH-A	brain:	n/a
35	chr4:187702884-187702934	GM12878	blood:	n/a
36	chr4:187702884-187702934	AoSMC	blood vessel:	n/a
37	chr4:187729190-187729240	SAEC	small airway:	n/a
38	chr4:187766591-187766641	ovcar-3	ovarian:	n/a
39	chr4:187766591-187766641	HCM	heart:	n/a
40	chr4:187762379-187762429	NH-A	brain:	n/a
41	chr4:187776068-187776118	MCF-7	breast:	n/a
42	chr4:187740664-187740714	HL-60	blood:	n/a
43	chr4:187702884-187702934	BJ	skin:	n/a
44	chr4:187783798-187783848	HUVEC	blood vessel:	n/a
45	chr4:187783798-187783848	HCM	heart:	n/a
46	chr4:187729190-187729240	HRE	kidney:	n/a
47	chr4:187765617-187765667	Hepatocyte	liver:	n/a
48	chr4:187729190-187729240	LNCaP	prostate:	n/a
49	chr4:187776068-187776118	PANC-1	pancreas:	n/a
50	chr4:187762256-187762306	RPTEC	kidney:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:187765177..187771006-chr4:187807000..187811310,9	K562	blood:
2	chr4:187749229..187751221-chr4:187752968..187755678,3	K562	blood:
3	chr4:187752478..187754438-chr4:187754618..187756611,2	K562	blood:
4	chr4:187749742..187751497-chr4:187825991..187828310,2	K562	blood:
5	chr4:187782071..187784960-chr4:187786338..187789221,2	K562	blood:
6	chr4:187682902..187684633-chr4:187696851..187698406,2	K562	blood:
7	chr4:187720294..187722380-chr4:187728478..187730946,2	K562	blood:
8	chr4:187648033..187649855-chr4:187758632..187760466,2	MCF-7	breast:
9	chr4:187766677..187768346-chr4:187783424..187785268,2	K562	blood:
10	chr4:187721104..187723680-chr4:187820349..187822022,2	K562	blood:
11	chr4:187647721..187650690-chr4:187732796..187735264,2	MCF-7	breast:
12	chr4:187675497..187677160-chr4:187761262..187763373,2	K562	blood:
13	chr4:187764771..187768253-chr4:187793042..187796524,4	K562	blood:
14	chr4:187673725..187675246-chr4:187709828..187712451,2	MCF-7	breast:
15	chr4:187740833..187742405-chr4:187744512..187747261,2	K562	blood:
16	chr4:187675288..187676998-chr4:187710830..187713799,2	K562	blood:
17	chr4:187676658..187680719-chr4:187744045..187748911,5	K562	blood:
18	chr4:187779063..187781190-chr4:187783722..187786241,2	K562	blood:
19	chr4:187762414..187767903-chr4:187771825..187775014,7	K562	blood:
20	chr4:187717769..187721707-chr4:187722275..187727445,6	K562	blood:
21	chr4:187704048..187707198-chr4:187707380..187710595,3	K562	blood:
22	chr4:187768093..187770928-chr4:187771108..187773724,3	K562	blood:
23	chr4:187419874..187422872-chr4:187765170..187767723,2	K562	blood:
24	chr4:187739285..187742127-chr4:187749398..187750937,2	K562	blood:
25	chr4:187742199..187747517-chr4:187748005..187751181,4	K562	blood:
26	chr4:187766677..187768346-chr4:187783424..187785268,2	K562	blood:
27	chr4:187676821..187679586-chr4:187746342..187750041,4	K562	blood:
28	chr4:187681629..187684562-chr4:187726628..187729444,2	K562	blood:
29	chr4:187768429..187770069-chr4:187807061..187809339,2	K562	blood:
30	chr4:187762414..187767903-chr4:187771825..187775014,7	K562	blood:
31	chr4:187712775..187715204-chr4:187721861..187723800,2	MCF-7	breast:
32	chr4:187668197..187669912-chr4:187699243..187701064,2	MCF-7	breast:
33	chr4:187718306..187722830-chr4:187723240..187727445,8	K562	blood:
34	chr4:187761346..187763070-chr4:187833747..187836237,2	K562	blood:
35	chr4:187704048..187707198-chr4:187707380..187710595,3	K562	blood:
36	chr4:187648173..187650328-chr4:187707410..187709180,2	MCF-7	breast:
37	chr4:187766368..187767880-chr4:187768124..187769704,2	K562	blood:
38	chr4:187680022..187681982-chr4:187780547..187782844,3	K562	blood:
39	chr4:187740833..187742405-chr4:187744512..187747261,2	K562	blood:
40	chr4:187675476..187679042-chr4:187722913..187726254,3	K562	blood:
41	chr4:187752478..187754438-chr4:187754618..187756611,2	K562	blood:
42	chr4:187720294..187722380-chr4:187728478..187730946,2	K562	blood:
43	chr4:187742199..187747517-chr4:187748005..187751181,4	K562	blood:
44	chr4:187644243..187647886-chr4:187765667..187770320,5	K562	blood:
45	chr4:187776828..187779410-chr4:187779609..187783099,3	K562	blood:
46	chr4:187765177..187768069-chr4:187809539..187811310,3	K562	blood:
47	chr13:84776815..84777795-chr4:187761106..187761969,2	HCT-116	colon:
48	chr4:187749279..187751049-chr4:187752829..187754468,2	K562	blood:
49	chr4:187717769..187721707-chr4:187722275..187727445,6	K562	blood:
50	chr4:187765345..187768109-chr4:187793611..187797439,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000252382	TF binding region
ENSG00000252382	CpG island
ENSG00000083857	chromatin interactions
ENSG00000251165	chromatin interactions
ENSG00000212387	chromatin interactions
ENSG00000168564	chromatin interactions
ENSG00000249539	chromatin interactions
ENSG00000252382	chromatin interactions

Extended variants
information (count: 3205 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3205 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9995398	chr4:187695564-187695565	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541324086	chr4:187695575-187695576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186261813	chr4:187695599-187695600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368419222	chr4:187695623-187695624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370627459	chr4:187695642-187695643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139452140	chr4:187695655-187695656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535594796	chr4:187695759-187695760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190733339	chr4:187695760-187695761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562808402	chr4:187695786-187695787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531944017	chr4:187695809-187695810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548445854	chr4:187695810-187695811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs464636	chr4:187695843-187695844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200327640	chr4:187695859-187695860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370056050	chr4:187695864-187695865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs57852925	chr4:187695866-187695867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79953339	chr4:187695867-187695868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs202157136	chr4:187695868-187695869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76844305	chr4:187695883-187695884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs117024442	chr4:187695922-187695923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547667118	chr4:187695958-187695959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570140693	chr4:187695960-187695961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183393390	chr4:187696004-187696005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549862923	chr4:187696006-187696007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569609457	chr4:187696074-187696075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9312350	chr4:187696077-187696078	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs9790398	chr4:187696094-187696095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564485627	chr4:187696096-187696097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534944631	chr4:187696100-187696101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558058168	chr4:187696112-187696113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577186769	chr4:187696117-187696118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186249598	chr4:187696144-187696145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4862732	chr4:187696158-187696159	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs562165936	chr4:187696162-187696163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576505119	chr4:187696170-187696171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541908307	chr4:187696179-187696180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190570254	chr4:187696194-187696195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144980382	chr4:187696195-187696196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541346450	chr4:187696209-187696210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs375020386	chr4:187696212-187696213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574060136	chr4:187696224-187696225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564590069	chr4:187696259-187696260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182747750	chr4:187696284-187696285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549559408	chr4:187696327-187696328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187773332	chr4:187696332-187696333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113172988	chr4:187696335-187696336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs192695087	chr4:187696403-187696404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563099020	chr4:187696452-187696453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183830974	chr4:187696457-187696458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565906376	chr4:187696475-187696476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534777682	chr4:187696486-187696487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
XY gonadal dysgenesis	20685758	CNVD
Schizophrenia	20967226	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:832 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187689000-187699200	Weak transcription	Fetal Intestine Small	intestine
2	chr4:187693000-187696800	Weak transcription	HepG2	liver
3	chr4:187693000-187697000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:187693200-187696200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:187693200-187697000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr4:187693400-187700200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:187693400-187701400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr4:187694400-187696600	Weak transcription	A549	lung
9	chr4:187696200-187696400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:187696400-187696800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:187696800-187697000	Enhancers	A549	lung
12	chr4:187696800-187697400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:187696800-187697400	Enhancers	HepG2	liver
14	chr4:187697000-187697400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:187697000-187697600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr4:187697400-187699000	Weak transcription	HepG2	liver
17	chr4:187697400-187701000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr4:187697600-187702600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr4:187699000-187699200	Enhancers	Small Intestine	intestine
20	chr4:187699000-187699600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:187699000-187705000	Enhancers	HepG2	liver
22	chr4:187699200-187699800	Enhancers	Fetal Intestine Small	intestine
23	chr4:187699200-187701000	Weak transcription	Small Intestine	intestine
24	chr4:187700000-187700200	Enhancers	Duodenum Mucosa	Duodenum
25	chr4:187700200-187700600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr4:187700200-187700800	Weak transcription	Duodenum Mucosa	Duodenum
27	chr4:187700600-187701000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:187700800-187702200	Enhancers	Duodenum Mucosa	Duodenum
29	chr4:187701000-187701800	Enhancers	Small Intestine	intestine
30	chr4:187701000-187702600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr4:187701000-187702600	Enhancers	Fetal Intestine Large	intestine
32	chr4:187701000-187702800	Enhancers	Fetal Intestine Small	intestine
33	chr4:187701000-187703400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:187701000-187703400	Enhancers	HMEC	breast
35	chr4:187701200-187702600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:187701200-187704000	Enhancers	NHEK	skin
37	chr4:187701400-187702400	Enhancers	Stomach Mucosa	stomach
38	chr4:187701400-187702600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:187701400-187702800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr4:187701600-187703400	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr4:187701800-187702400	Weak transcription	Small Intestine	intestine
42	chr4:187701800-187703000	Enhancers	K562	blood
43	chr4:187702000-187703200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr4:187702200-187702600	Enhancers	NHLF	lung
45	chr4:187702400-187702600	Enhancers	Small Intestine	intestine
46	chr4:187702400-187702800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:187702400-187702800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:187702400-187703000	Enhancers	Fetal Lung	lung
49	chr4:187702400-187703000	Enhancers	NH-A	brain
50	chr4:187702400-187703600	Weak transcription	Stomach Mucosa	stomach

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