Variant report

Variant	nsv594611
Chromosome Location	chr4:70261746-70383991
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:965)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:965 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70383793-70384506	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70359216-70359556	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70350802-70351141	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70324166-70324568	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:70361428-70361936	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:70296492-70296914	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:70296492-70296919	K562	blood:	n/a	n/a
8	ARID3A	chr4:70274315-70274516	HepG2	liver:	n/a	n/a
9	ATF1	chr4:70296489-70296914	K562	blood:	n/a	n/a
10	ATF2	chr4:70333524-70333998	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr4:70296552-70296826	A549	lung:	n/a	n/a
12	ATF3	chr4:70296558-70296973	A549	lung:	n/a	n/a
13	ATF3	chr4:70296574-70296796	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr4:70296499-70296777	HepG2	liver:	n/a	n/a
15	BACH1	chr4:70296489-70296908	K562	blood:	n/a	n/a
16	BATF	chr4:70296590-70296824	GM12878	blood:	n/a	n/a
17	BATF	chr4:70367562-70367758	GM12878	blood:	n/a	chr4:70367695-70367706
18	BATF	chr4:70296589-70296863	GM12878	blood:	n/a	chr4:70296823-70296832
19	BCL11A	chr4:70296596-70296779	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:70296603-70296770	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr4:70296569-70296786	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL11A	chr4:70296551-70296867	GM12878	blood:	n/a	n/a
23	BCL3	chr4:70296436-70296843	A549	lung:	n/a	n/a
24	BCL3	chr4:70296548-70296829	A549	lung:	n/a	n/a
25	BCLAF1	chr4:70296549-70296826	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:70296483-70296924	K562	blood:	n/a	n/a
27	BHLHE40	chr4:70296485-70296909	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:70361410-70361902	HepG2	liver:	n/a	n/a
29	BRCA1	chr4:70296483-70296909	HepG2	liver:	n/a	n/a
30	BRCA1	chr4:70296486-70296910	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr4:70296484-70296924	GM12878	blood:	n/a	n/a
32	CBX3	chr4:70290507-70290706	K562	blood:	n/a	n/a
33	CCNT2	chr4:70296445-70296895	K562	blood:	n/a	n/a
34	CEBPB	chr4:70296589-70296760	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:70339506-70339743	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:70333789-70333989	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:70324164-70324515	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:70324212-70324508	HepG2	liver:	n/a	n/a
39	CEBPB	chr4:70302923-70302937	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:70296570-70296806	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:70361394-70361769	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:70324137-70324588	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:70350737-70351236	HepG2	liver:	n/a	chr4:70351083-70351094
44	CEBPB	chr4:70359060-70359353	A549	lung:	n/a	chr4:70359161-70359174 chr4:70359163-70359174 chr4:70359161-70359174 chr4:70359161-70359172 chr4:70359235-70359246
45	CEBPB	chr4:70276530-70276708	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:70361393-70361913	HepG2	liver:	n/a	n/a
47	CEBPB	chr4:70371476-70371676	HepG2	liver:	n/a	chr4:70371515-70371526
48	CEBPB	chr4:70324294-70324494	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr4:70359098-70359325	K562	blood:	n/a	chr4:70359161-70359174 chr4:70359163-70359174 chr4:70359161-70359174 chr4:70359161-70359172 chr4:70359235-70359246
50	CEBPB	chr4:70296486-70296925	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70346347-70346397	H1-hESC	embryonic stem cell:	embryo
2	chr4:70346347-70346397	GM06990	blood:	n/a
3	chr4:70346347-70346397	HEEpiC	esophagus:	n/a
4	chr4:70346347-70346397	NHDF-neo	bronchial:	n/a
5	chr4:70361062-70361112	BJ	skin:	n/a
6	chr4:70346347-70346397	Jurkat	blood:	n/a
7	chr4:70346347-70346397	AG04449	skin:	fetal
8	chr4:70361062-70361112	GM19239	blood:	n/a
9	chr4:70346347-70346397	AoSMC	blood vessel:	n/a
10	chr4:70346347-70346397	Caco-2	colon:	n/a
11	chr4:70361062-70361112	HRCEpiC	kidney:	n/a
12	chr4:70346347-70346397	BE2_C	brain:	n/a
13	chr4:70361062-70361112	MCF-7	breast:	n/a
14	chr4:70361062-70361112	AG04450	lung:	fetal
15	chr4:70361062-70361112	Caco-2	colon:	n/a
16	chr4:70346347-70346397	HNPCEpiC	eye:	n/a
17	chr4:70361062-70361112	CMK	blood:	n/a
18	chr4:70346347-70346397	AG09319	gingival:	n/a
19	chr4:70346347-70346397	NB4	blood:	n/a
20	chr4:70361062-70361112	HCPEpiC	choroid plexus:	n/a
21	chr4:70346347-70346397	Hela-S3	cervix:	n/a
22	chr4:70346347-70346397	HCM	heart:	n/a
23	chr4:70361062-70361112	AG04449	skin:	fetal
24	chr4:70361062-70361112	Hepatocyte	liver:	n/a
25	chr4:70346347-70346397	BJ	skin:	n/a
26	chr4:70346347-70346397	GM12892	blood:	n/a
27	chr4:70361062-70361112	T-47D	breast:	n/a
28	chr4:70361062-70361112	Jurkat	blood:	n/a
29	chr4:70361062-70361112	PANC-1	pancreas:	n/a
30	chr4:70346347-70346397	K562	blood:	n/a
31	chr4:70361062-70361112	GM12891	blood:	n/a
32	chr4:70361062-70361112	HL-60	blood:	n/a
33	chr4:70346347-70346397	A549	lung:	n/a
34	chr4:70346347-70346397	NT2-D1	testis:	n/a
35	chr4:70361062-70361112	PrEC	prostate:	n/a
36	chr4:70361062-70361112	GM12878	blood:	n/a
37	chr4:70361062-70361112	AG09309	skin:	n/a
38	chr4:70361062-70361112	LNCaP	prostate:	n/a
39	chr4:70361062-70361112	H1-hESC	embryonic stem cell:	embryo
40	chr4:70361062-70361112	SK-N-MC	brain:	n/a
41	chr4:70346347-70346397	SK-N-MC	brain:	n/a
42	chr4:70346347-70346397	AG09309	skin:	n/a
43	chr4:70346347-70346397	AG04450	lung:	fetal
44	chr4:70346347-70346397	ECC-1	luminal epithelium:	n/a
45	chr4:70346347-70346397	HCF	heart:	n/a
46	chr4:70346347-70346397	U87	brain:	n/a
47	chr4:70361062-70361112	HCM	heart:	n/a
48	chr4:70346347-70346397	SK-N-SH	brain:	n/a
49	chr4:70346347-70346397	GM12891	blood:	n/a
50	chr4:70346347-70346397	HepG2	liver:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:133011384..133014243-chr4:70295163..70298145,2	K562	blood:
2	chr19:24184130..24184632-chr4:70296678..70297183,2	MCF-7	breast:
3	chr4:70262708..70264895-chr4:70280098..70283006,2	K562	blood:
4	chr2:133038471..133039156-chr4:70296229..70297178,3	MCF-7	breast:
5	chr2:169797130..169797902-chr4:70311918..70312713,2	MCF-7	breast:
6	chr19:36066562..36067220-chr4:70296617..70297159,2	MCF-7	breast:
7	chr4:70379330..70381215-chr4:70382030..70384687,2	K562	blood:
8	chr12:6797888..6800431-chr4:70351986..70354075,2	MCF-7	breast:
9	chr21:9824058..9826515-chr4:70295211..70298169,2	K562	blood:
10	chr4:70262708..70264895-chr4:70280098..70283006,2	K562	blood:
11	chr21:9825015..9827465-chr4:70296669..70298179,2	K562	blood:
12	chr4:70296625..70297182-chr6:133594074..133594625,3	MCF-7	breast:
13	chr20:52578439..52580096-chr4:70380828..70382348,2	MCF-7	breast:
14	chr4:70383119..70384022-chr4:70482515..70483454,3	MCF-7	breast:
15	chr19:24183615..24184637-chr4:70296138..70296644,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-5	chr4:70272649-70273373	NONHSAT096764
2	lnc-UGT2B28-6	chr4:70304044-70304260	NONHSAT096765
3	lnc-UGT2B28-7	chr4:70315732-70315864	NONHSAT096766
4	lnc-UGT2B28-6	chr4:70303075-70303156	NONHSAT096765
5	lnc-UGT2B28-7	chr4:70317229-70317331	NONHSAT096766
6	lnc-UGT2B28-6	chr4:70306600-70306768	NONHSAT096765

No data

Variant related genes	Relation type
ENSG00000250828	TF binding region
ENSG00000249956	TF binding region
UGT2B4	TF binding region
ENSG00000248824	TF binding region
ENSG00000249686	TF binding region
ENSG00000264696	TF binding region
ENSG00000250828	CpG island
ENSG00000249956	CpG island
UGT2B4	CpG island
ENSG00000248824	CpG island
ENSG00000249686	CpG island
ENSG00000264696	CpG island
ENSG00000264063	chromatin interactions
ENSG00000264462	chromatin interactions
ENSG00000248886	chromatin interactions
ENSG00000126746	chromatin interactions

Extended variants
information (count: 2457 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2457 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536980736	chr4:70265033-70265034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs62306698	chr4:70265047-70265048	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs192490741	chr4:70265090-70265091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538802047	chr4:70265107-70265108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183433985	chr4:70265108-70265109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs17146890	chr4:70265111-70265112	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs189092359	chr4:70265118-70265119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144893174	chr4:70265127-70265128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138727989	chr4:70265164-70265165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574716165	chr4:70265169-70265170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543756750	chr4:70265175-70265176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192149778	chr4:70265178-70265179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs59380046	chr4:70265195-70265196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184570963	chr4:70265204-70265205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559271050	chr4:70265231-70265232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528221541	chr4:70265259-70265260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112115105	chr4:70265289-70265290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs386675681	chr4:70265290-70265291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111239996	chr4:70265292-70265293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530390734	chr4:70265332-70265333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550069944	chr4:70265334-70265335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547128789	chr4:70265350-70265351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570063126	chr4:70265351-70265352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540870134	chr4:70267652-70267653	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs543015932	chr4:70267676-70267677	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs574115235	chr4:70267680-70267681	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs182234611	chr4:70270040-70270041	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs568614232	chr4:70270046-70270047	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs186897894	chr4:70270049-70270050	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs550730454	chr4:70270084-70270085	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs570801792	chr4:70270108-70270109	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs539372279	chr4:70270124-70270125	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs111415606	chr4:70270620-70270621	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs542517861	chr4:70270623-70270624	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs371669964	chr4:70270628-70270629	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs187621176	chr4:70270644-70270645	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs562288171	chr4:70270658-70270659	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs112221746	chr4:70270664-70270665	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs535581179	chr4:70270671-70270672	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs113281075	chr4:70270675-70270676	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs192649089	chr4:70270681-70270682	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs544831603	chr4:70270938-70270939	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs564506899	chr4:70270955-70270956	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs578070320	chr4:70270956-70270957	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs7671162	chr4:70270965-70270966	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs574780260	chr4:70272664-70272665	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs543290674	chr4:70272712-70272713	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs563480183	chr4:70272713-70272714	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs200560590	chr4:70272794-70272795	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs56057328	chr4:70272830-70272831	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	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
Multiple myeloma	16616336	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Oral cancer	21386901	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70265000-70265400	Enhancers	Fetal Heart	heart
2	chr4:70295800-70296400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr4:70296400-70296800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:70296400-70297000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
5	chr4:70296400-70297000	ZNF genes & repeats	Gastric	stomach
6	chr4:70296400-70297000	ZNF genes & repeats	Right Atrium	heart
7	chr4:70296400-70297000	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
8	chr4:70296400-70297000	Flanking Bivalent TSS/Enh	Spleen	Spleen
9	chr4:70296600-70296800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr4:70296600-70296800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
13	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:70296600-70296800	ZNF genes & repeats	Primary B cells from cord blood	blood
15	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
16	chr4:70296600-70296800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
17	chr4:70296600-70296800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
18	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
19	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
20	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Primary Natural Killer cells fromperipheralblood	blood
21	chr4:70296600-70296800	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
22	chr4:70296600-70296800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
23	chr4:70296600-70296800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr4:70296600-70296800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr4:70296600-70296800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr4:70296600-70296800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr4:70296600-70296800	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
29	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Aorta	Aorta
30	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
31	chr4:70296600-70296800	ZNF genes & repeats	Brain Germinal Matrix	brain
32	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
33	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Brain Inferior Temporal Lobe	brain
34	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Brain Substantia Nigra	brain
35	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
36	chr4:70296600-70296800	Bivalent Enhancer	Fetal Heart	heart
37	chr4:70296600-70296800	ZNF genes & repeats	Fetal Kidney	kidney
38	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
39	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Placenta	Placenta
40	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
41	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Ovary	ovary
42	chr4:70296600-70296800	ZNF genes & repeats	Placenta Amnion	Placenta Amnion
43	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
44	chr4:70296600-70296800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
45	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
46	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
47	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Small Intestine	intestine
48	chr4:70296600-70296800	ZNF genes & repeats	Thymus	Thymus
49	chr4:70296600-70296800	ZNF genes & repeats	HUVEC	blood vessel
50	chr4:70296600-70296800	ZNF genes & repeats	NHDF-Ad	bronchial

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