Variant report

Variant	nsv1005338
Chromosome Location	chr4:87023398-87108555
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:267)
CpG islands
(count:305)
Chromatin interactive
region (count:14)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:87029865-87030369	HepG2	liver:	n/a	n/a
2	BHLHE40	chr4:87030030-87030251	HepG2	liver:	n/a	n/a
3	CEBPB	chr4:87039044-87039507	A549	lung:	n/a	n/a
4	CEBPB	chr4:87080544-87080605	IMR90	lung:	n/a	n/a
5	CEBPB	chr4:87063544-87063833	A549	lung:	n/a	chr4:87063684-87063695
6	CEBPB	chr4:87108462-87108618	A549	lung:	n/a	n/a
7	CEBPB	chr4:87063517-87063828	IMR90	lung:	n/a	chr4:87063684-87063695
8	CEBPB	chr4:87080285-87080666	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:87063552-87063827	HepG2	liver:	n/a	chr4:87063684-87063695
10	CEBPB	chr4:87055574-87055650	K562	blood:	n/a	chr4:87055591-87055602 chr4:87055593-87055606 chr4:87055591-87055602 chr4:87055595-87055606
11	CEBPB	chr4:87105460-87105731	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr4:87063561-87063863	K562	blood:	n/a	chr4:87063684-87063695
13	CEBPB	chr4:87108365-87108678	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:87039260-87039438	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:87108494-87108549	K562	blood:	n/a	n/a
16	CTCF	chr4:87099220-87099370	HPAF	blood vessel:	n/a	chr4:87099308-87099329 chr4:87099313-87099331
17	CTCF	chr4:87069562-87069571	GM13976	blood:	n/a	n/a
18	CTCF	chr4:87081504-87081582	Fibrobl	skin:	n/a	n/a
19	CTCF	chr4:87069577-87069592	GM13976	blood:	n/a	n/a
20	CTCF	chr4:87036507-87036542	GM10266	blood:	n/a	n/a
21	CTCF	chr4:87099280-87099430	WI-38	lung:	n/a	chr4:87099308-87099329 chr4:87099313-87099331
22	CTCF	chr4:87099160-87099310	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr4:87074931-87074990	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr4:87089364-87089407	MCF-7	breast:	n/a	n/a
25	CTCF	chr4:87038180-87038330	AG04449	skin:	n/a	n/a
26	CTCF	chr4:87036612-87036649	LNCaP	prostate:	n/a	n/a
27	CTCF	chr4:87094959-87095028	GM20000	blood:	n/a	n/a
28	CTCF	chr4:87035094-87035127	Lung_OC	lung:	n/a	n/a
29	CTCF	chr4:87099180-87099330	HPAF	blood vessel:	n/a	chr4:87099308-87099329
30	CTCF	chr4:87044740-87044890	AG10803	skin:	n/a	n/a
31	E2F4	chr4:87107864-87107989	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr4:87067895-87068014	MCF10A-Er-Src	breast:	n/a	n/a
33	EP300	chr4:87063569-87063960	SK-N-SH_RA	brain:	n/a	n/a
34	EP300	chr4:87051630-87052160	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr4:87029348-87029620	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr4:87063566-87063988	SK-N-SH_RA	brain:	n/a	n/a
37	EP300	chr4:87052593-87052985	SK-N-SH_RA	brain:	n/a	chr4:87052736-87052750
38	EP300	chr4:87106816-87107373	SK-N-SH	brain:	n/a	n/a
39	EP300	chr4:87070690-87070979	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr4:87038541-87039650	SK-N-SH	brain:	n/a	n/a
41	EP300	chr4:87070615-87070998	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr4:87039007-87039593	A549	lung:	n/a	n/a
43	EP300	chr4:87038594-87039616	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr4:87102706-87103125	A549	lung:	n/a	chr4:87102798-87102812
45	EP300	chr4:87051413-87052289	SK-N-SH	brain:	n/a	n/a
46	EP300	chr4:87051517-87052373	SK-N-SH	brain:	n/a	n/a
47	EP300	chr4:87050722-87051046	SK-N-SH_RA	brain:	n/a	chr4:87050984-87050998
48	EP300	chr4:87029309-87029842	SK-N-SH	brain:	n/a	n/a
49	EP300	chr4:87051587-87052161	SK-N-SH_RA	brain:	n/a	n/a
50	EP300	chr4:87038477-87040418	SK-N-SH	brain:	n/a	chr4:87039897-87039911 chr4:87039891-87039905

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:87030123-87030173	ProgFib	skin:	n/a
2	chr4:87040423-87040473	Hepatocyte	liver:	n/a
3	chr4:87040423-87040473	GM12878	blood:	n/a
4	chr4:87040423-87040473	Caco-2	colon:	n/a
5	chr4:87030123-87030173	HL-60	blood:	n/a
6	chr4:87030123-87030173	PANC-1	pancreas:	n/a
7	chr4:87030123-87030173	NH-A	brain:	n/a
8	chr4:87056153-87056203	NH-A	brain:	n/a
9	chr4:87040423-87040473	PrEC	prostate:	n/a
10	chr4:87040423-87040473	GM12892	blood:	n/a
11	chr4:87028602-87028652	H1-hESC	embryonic stem cell:	embryo
12	chr4:87040423-87040473	SKMC	muscle:	n/a
13	chr4:87028602-87028652	HepG2	liver:	n/a
14	chr4:87028501-87028551	IMR90	lung:	fetal
15	chr4:87040423-87040473	AoSMC	blood vessel:	n/a
16	chr4:87030123-87030173	Hepatocyte	liver:	n/a
17	chr4:87030123-87030173	HRCEpiC	kidney:	n/a
18	chr4:87056153-87056203	HEEpiC	esophagus:	n/a
19	chr4:87040423-87040473	ProgFib	skin:	n/a
20	chr4:87028501-87028551	MCF10A-Er-Src	breast:	n/a
21	chr4:87028602-87028652	HRPEpiC	eye:	n/a
22	chr4:87040423-87040473	AG10803	skin:	n/a
23	chr4:87056153-87056203	SK-N-MC	brain:	n/a
24	chr4:87056153-87056203	HMEC	breast:	n/a
25	chr4:87040423-87040473	BE2_C	brain:	n/a
26	chr4:87030123-87030173	AoSMC	blood vessel:	n/a
27	chr4:87028602-87028652	HEK293	kidney:	embryo
28	chr4:87030123-87030173	CMK	blood:	n/a
29	chr4:87056153-87056203	HCF	heart:	n/a
30	chr4:87030123-87030173	HUVEC	blood vessel:	n/a
31	chr4:87030123-87030173	BE2_C	brain:	n/a
32	chr4:87028602-87028652	A549	lung:	n/a
33	chr4:87028602-87028652	AG09319	gingival:	n/a
34	chr4:87056153-87056203	MCF10A-Er-Src	breast:	n/a
35	chr4:87040423-87040473	HL-60	blood:	n/a
36	chr4:87056153-87056203	PANC-1	pancreas:	n/a
37	chr4:87040423-87040473	HRCEpiC	kidney:	n/a
38	chr4:87056153-87056203	U87	brain:	n/a
39	chr4:87030123-87030173	NT2-D1	testis:	n/a
40	chr4:87028501-87028551	A549	lung:	n/a
41	chr4:87028501-87028551	RPTEC	kidney:	n/a
42	chr4:87028602-87028652	AoSMC	blood vessel:	n/a
43	chr4:87030123-87030173	MCF10A-Er-Src	breast:	n/a
44	chr4:87028602-87028652	Hela-S3	cervix:	n/a
45	chr4:87030123-87030173	Caco-2	colon:	n/a
46	chr4:87056153-87056203	GM19239	blood:	n/a
47	chr4:87028501-87028551	AG09309	skin:	n/a
48	chr4:87030123-87030173	GM06990	blood:	n/a
49	chr4:87030123-87030173	SAEC	small airway:	n/a
50	chr4:87056153-87056203	CMK	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:87079015..87081853-chr4:87083542..87085468,2	K562	blood:
2	chr4:87074554..87076995-chr4:87081060..87082909,2	MCF-7	breast:
3	chr4:87068101..87070840-chr4:87077987..87079819,2	MCF-7	breast:
4	chr4:87070864..87073086-chr4:87075454..87077437,2	K562	blood:
5	chr4:87070864..87073086-chr4:87075454..87077437,2	K562	blood:
6	chr4:87070864..87072590-chr4:87074186..87076954,2	K562	blood:
7	chr4:87024355..87027343-chr4:87027765..87029282,2	MCF-7	breast:
8	chr4:87068101..87070840-chr4:87077987..87079819,2	MCF-7	breast:
9	chr4:87074554..87076995-chr4:87081060..87082909,2	MCF-7	breast:
10	chr4:87079015..87081853-chr4:87083542..87085468,2	K562	blood:
11	chr4:87048655..87051037-chr4:87083679..87085994,2	MCF-7	breast:
12	chr4:87070864..87072590-chr4:87074186..87076954,2	K562	blood:
13	chr4:87024355..87027343-chr4:87027765..87029282,2	MCF-7	breast:
14	chr4:87048655..87051037-chr4:87083679..87085994,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC10A6-4	chr4:87085599-87085718	NONHSAT097276
2	lnc-ARHGAP24-1	chr4:87041137-87041754	ENSG00000250062.1
3	lnc-ARHGAP24-1	chr4:87048745-87048940	NONHSAT097275
4	lnc-SLC10A6-4	chr4:87097140-87097232	NONHSAT097276
5	lnc-ARHGAP24-1	chr4:87041137-87041754	ENSG00000250062.1
6	lnc-ARHGAP24-1	chr4:87048745-87048841	ENSG00000250062.1
7	lnc-ARHGAP24-1	chr4:87040867-87041036	ENSG00000250062.1
8	lnc-ARHGAP24-1	chr4:87040879-87041036	NONHSAT097275
9	lnc-ARHGAP24-1	chr4:87039065-87039115	ENSG00000250062.1
10	lnc-ARHGAP24-1	chr4:87048745-87048853	ENSG00000250062.1
11	lnc-ARHGAP24-1	chr4:87041137-87041754	NONHSAT097275

No data

Variant related genes	Relation type
MAPK10	TF binding region
ENSG00000250062	TF binding region
MAPK10	CpG island
ENSG00000250062	CpG island
ENSG00000109339	chromatin interactions

Extended variants
information (count: 2966 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2966 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148550581	chr4:87023506-87023507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574308088	chr4:87023533-87023534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564241893	chr4:87023537-87023538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372736928	chr4:87023552-87023553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528523952	chr4:87023599-87023600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546686916	chr4:87023613-87023614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12646571	chr4:87023654-87023655	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs375299082	chr4:87023676-87023677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548483295	chr4:87023682-87023683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145681898	chr4:87023696-87023697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537253823	chr4:87023702-87023703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558744945	chr4:87023705-87023706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570652219	chr4:87023709-87023710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534755393	chr4:87023715-87023716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553081345	chr4:87023718-87023719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574407486	chr4:87023727-87023728	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147735340	chr4:87023759-87023760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557654096	chr4:87023766-87023767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113353093	chr4:87023770-87023771	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185923687	chr4:87023818-87023819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564378551	chr4:87023828-87023829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113890574	chr4:87023865-87023866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112240182	chr4:87023987-87023988	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78841001	chr4:87023997-87023998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529310145	chr4:87024003-87024004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550657443	chr4:87024027-87024028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7688633	chr4:87024033-87024034	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs191575072	chr4:87024083-87024084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552498340	chr4:87024115-87024116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570686210	chr4:87024134-87024135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371026918	chr4:87024149-87024150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374537659	chr4:87024170-87024171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563777764	chr4:87024228-87024229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34063796	chr4:87024229-87024230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs202025861	chr4:87024232-87024233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140180714	chr4:87024234-87024235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112946101	chr4:87024240-87024241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534792965	chr4:87024241-87024242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546730323	chr4:87024264-87024265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373735532	chr4:87024270-87024271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368198983	chr4:87024271-87024272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371450495	chr4:87024272-87024273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201901459	chr4:87024290-87024291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565102877	chr4:87024293-87024294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138883015	chr4:87024360-87024361	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs535434553	chr4:87024372-87024373	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs28529458	chr4:87024409-87024410	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs575167092	chr4:87024410-87024411	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs7693923	chr4:87024433-87024434	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs150314520	chr4:87024475-87024476	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
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
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	20459617	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:87004000-87028400	Weak transcription	Stomach Smooth Muscle	stomach
2	chr4:87005000-87050400	Weak transcription	Brain Angular Gyrus	brain
3	chr4:87005400-87028200	Weak transcription	Ovary	ovary
4	chr4:87005400-87028400	Weak transcription	Fetal Stomach	stomach
5	chr4:87005600-87026200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr4:87005600-87031200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr4:87005600-87035200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:87009200-87027400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr4:87010800-87035800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr4:87011400-87035600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr4:87011800-87028400	Weak transcription	Fetal Lung	lung
12	chr4:87015600-87024400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:87015800-87024400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr4:87016600-87028200	Weak transcription	Brain Hippocampus Middle	brain
15	chr4:87021400-87023400	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr4:87022200-87023400	Enhancers	Fetal Brain Male	brain
17	chr4:87023000-87023400	Strong transcription	Brain Anterior Caudate	brain
18	chr4:87023000-87023400	Strong transcription	Brain Inferior Temporal Lobe	brain
19	chr4:87023200-87023400	Enhancers	A549	lung
20	chr4:87023400-87026400	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr4:87023400-87026600	Weak transcription	Fetal Brain Male	brain
22	chr4:87023400-87038800	Weak transcription	Brain Anterior Caudate	brain
23	chr4:87024400-87024800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:87024400-87024800	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr4:87024800-87025600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:87025600-87029000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:87026000-87029800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr4:87026600-87026800	Enhancers	Fetal Brain Male	brain
29	chr4:87026800-87032600	Weak transcription	Fetal Brain Male	brain
30	chr4:87027000-87027200	Enhancers	Aorta	Aorta
31	chr4:87027200-87028200	Weak transcription	Aorta	Aorta
32	chr4:87027400-87029400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr4:87027800-87028000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr4:87027800-87029800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr4:87027800-87029800	Enhancers	Osteobl	bone
36	chr4:87027800-87030000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr4:87028000-87029000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr4:87028200-87028400	Active TSS	Aorta	Aorta
39	chr4:87028200-87028600	Flanking Active TSS	Ovary	ovary
40	chr4:87028200-87028800	Enhancers	Colon Smooth Muscle	Colon
41	chr4:87028200-87029600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr4:87028200-87030000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr4:87028400-87028600	Flanking Active TSS	Aorta	Aorta
44	chr4:87028400-87028600	Enhancers	Fetal Lung	lung
45	chr4:87028400-87028600	Enhancers	Fetal Stomach	stomach
46	chr4:87028400-87028600	Active TSS	Stomach Smooth Muscle	stomach
47	chr4:87028600-87028800	Enhancers	Ovary	ovary
48	chr4:87028600-87030000	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr4:87029000-87029800	Enhancers	NHDF-Ad	bronchial
50	chr4:87029000-87030000	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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