Variant report

Variant	nsv1003378
Chromosome Location	chr4:70285896-70354601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:655)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:655 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70324166-70324568	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70296492-70296919	K562	blood:	n/a	n/a
3	ARID3A	chr4:70296492-70296914	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70350802-70351141	HepG2	liver:	n/a	n/a
5	ATF1	chr4:70296489-70296914	K562	blood:	n/a	n/a
6	ATF2	chr4:70333524-70333998	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr4:70296499-70296777	HepG2	liver:	n/a	n/a
8	ATF3	chr4:70296574-70296796	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr4:70296552-70296826	A549	lung:	n/a	n/a
10	ATF3	chr4:70296558-70296973	A549	lung:	n/a	n/a
11	BACH1	chr4:70296489-70296908	K562	blood:	n/a	n/a
12	BATF	chr4:70296590-70296824	GM12878	blood:	n/a	n/a
13	BATF	chr4:70296589-70296863	GM12878	blood:	n/a	chr4:70296823-70296832
14	BCL11A	chr4:70296603-70296770	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr4:70296569-70296786	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr4:70296596-70296779	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:70296551-70296867	GM12878	blood:	n/a	n/a
18	BCL3	chr4:70296548-70296829	A549	lung:	n/a	n/a
19	BCL3	chr4:70296436-70296843	A549	lung:	n/a	n/a
20	BCLAF1	chr4:70296549-70296826	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:70296485-70296909	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:70296483-70296924	K562	blood:	n/a	n/a
23	BRCA1	chr4:70296483-70296909	HepG2	liver:	n/a	n/a
24	BRCA1	chr4:70296486-70296910	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr4:70296484-70296924	GM12878	blood:	n/a	n/a
26	CBX3	chr4:70290507-70290706	K562	blood:	n/a	n/a
27	CCNT2	chr4:70296445-70296895	K562	blood:	n/a	n/a
28	CEBPB	chr4:70347375-70347559	A549	lung:	n/a	n/a
29	CEBPB	chr4:70296589-70296760	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:70296570-70296806	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:70350737-70351236	HepG2	liver:	n/a	chr4:70351083-70351094
32	CEBPB	chr4:70333789-70333989	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr4:70324164-70324515	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:70296486-70296925	K562	blood:	n/a	n/a
35	CEBPB	chr4:70302923-70302937	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:70324294-70324494	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:70324169-70324482	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:70339506-70339743	HepG2	liver:	n/a	n/a
39	CEBPB	chr4:70324137-70324588	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:70324212-70324508	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:70319378-70319596	HepG2	liver:	n/a	chr4:70319545-70319556
42	CEBPB	chr4:70296492-70296908	Hela-S3	cervix:	n/a	n/a
43	CEBPD	chr4:70296588-70296895	K562	blood:	n/a	n/a
44	CEBPD	chr4:70296548-70296776	HepG2	liver:	n/a	n/a
45	CEBPD	chr4:70296470-70296789	HepG2	liver:	n/a	n/a
46	CHD1	chr4:70296484-70296924	GM12878	blood:	n/a	n/a
47	CHD1	chr4:70338556-70338566	GM12878	blood:	n/a	n/a
48	CHD2	chr4:70296447-70296925	HepG2	liver:	n/a	n/a
49	CHD2	chr4:70296483-70296909	K562	blood:	n/a	n/a
50	CHD2	chr4:70296490-70296924	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70346347-70346397	HEK293	kidney:	embryo
2	chr4:70346347-70346397	Jurkat	blood:	n/a
3	chr4:70346347-70346397	HEEpiC	esophagus:	n/a
4	chr4:70346347-70346397	IMR90	lung:	fetal
5	chr4:70346347-70346397	NT2-D1	testis:	n/a
6	chr4:70346347-70346397	H1-hESC	embryonic stem cell:	embryo
7	chr4:70346347-70346397	NB4	blood:	n/a
8	chr4:70346347-70346397	HMEC	breast:	n/a
9	chr4:70346347-70346397	PrEC	prostate:	n/a
10	chr4:70346347-70346397	U87	brain:	n/a
11	chr4:70346347-70346397	SK-N-MC	brain:	n/a
12	chr4:70346347-70346397	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:70346347-70346397	ProgFib	skin:	n/a
14	chr4:70346347-70346397	SKMC	muscle:	n/a
15	chr4:70346347-70346397	Caco-2	colon:	n/a
16	chr4:70346347-70346397	HepG2	liver:	n/a
17	chr4:70346347-70346397	HIPEpiC	eye:	n/a
18	chr4:70346347-70346397	HCT-116	colon:	n/a
19	chr4:70346347-70346397	AG04450	lung:	fetal
20	chr4:70346347-70346397	K562	blood:	n/a
21	chr4:70346347-70346397	SK-N-SH	brain:	n/a
22	chr4:70346347-70346397	HRE	kidney:	n/a
23	chr4:70346347-70346397	NHBE	bronchial:	n/a
24	chr4:70346347-70346397	HAEpiC	amniotic membrane:	n/a
25	chr4:70346347-70346397	BE2_C	brain:	n/a
26	chr4:70346347-70346397	HCPEpiC	choroid plexus:	n/a
27	chr4:70346347-70346397	PANC-1	pancreas:	n/a
28	chr4:70346347-70346397	AG10803	skin:	n/a
29	chr4:70346347-70346397	HUVEC	blood vessel:	n/a
30	chr4:70346347-70346397	RPTEC	kidney:	n/a
31	chr4:70346347-70346397	SAEC	small airway:	n/a
32	chr4:70346347-70346397	GM12891	blood:	n/a
33	chr4:70346347-70346397	SK-N-SH_RA	brain:	n/a
34	chr4:70346347-70346397	AG04449	skin:	fetal
35	chr4:70346347-70346397	GM12878	blood:	n/a
36	chr4:70346347-70346397	A549	lung:	n/a
37	chr4:70346347-70346397	AG09319	gingival:	n/a
38	chr4:70346347-70346397	HCM	heart:	n/a
39	chr4:70346347-70346397	Hela-S3	cervix:	n/a
40	chr4:70346347-70346397	HNPCEpiC	eye:	n/a
41	chr4:70346347-70346397	BJ	skin:	n/a
42	chr4:70346347-70346397	GM06990	blood:	n/a
43	chr4:70346347-70346397	HCF	heart:	n/a
44	chr4:70346347-70346397	HRPEpiC	eye:	n/a
45	chr4:70346347-70346397	AoSMC	blood vessel:	n/a
46	chr4:70346347-70346397	CMK	blood:	n/a
47	chr4:70346347-70346397	HRCEpiC	kidney:	n/a
48	chr4:70346347-70346397	Hepatocyte	liver:	n/a
49	chr4:70346347-70346397	ovcar-3	ovarian:	n/a
50	chr4:70346347-70346397	HL-60	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:133038471..133039156-chr4:70296229..70297178,3	MCF-7	breast:
2	chr12:6797888..6800431-chr4:70351986..70354075,2	MCF-7	breast:
3	chr19:24183615..24184637-chr4:70296138..70296644,3	K562	blood:
4	chr19:36066562..36067220-chr4:70296617..70297159,2	MCF-7	breast:
5	chr4:70296625..70297182-chr6:133594074..133594625,3	MCF-7	breast:
6	chr21:9824058..9826515-chr4:70295211..70298169,2	K562	blood:
7	chr19:24184130..24184632-chr4:70296678..70297183,2	MCF-7	breast:
8	chr2:133011384..133014243-chr4:70295163..70298145,2	K562	blood:
9	chr2:169797130..169797902-chr4:70311918..70312713,2	MCF-7	breast:
10	chr21:9825015..9827465-chr4:70296669..70298179,2	K562	blood:

(count:5 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 1491 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1491 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111969346	chr4:70295211-70295212	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs187187791	chr4:70295219-70295220	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs373133897	chr4:70295220-70295221	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs375775052	chr4:70295249-70295250	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs555695047	chr4:70295277-70295278	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs370114792	chr4:70295284-70295285	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs200647443	chr4:70295309-70295310	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs372206467	chr4:70295310-70295311	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs55893442	chr4:70295313-70295314	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs10010389	chr4:70295321-70295322	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs538185704	chr4:70295329-70295330	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs558023755	chr4:70295332-70295333	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs374126422	chr4:70295348-70295349	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs578131066	chr4:70295379-70295380	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs2736495	chr4:70295387-70295388	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs540804750	chr4:70295421-70295422	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs560397303	chr4:70295427-70295428	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs192850187	chr4:70295461-70295462	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs542667012	chr4:70295486-70295487	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs371219872	chr4:70295518-70295519	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs551728592	chr4:70295541-70295542	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs536531638	chr4:70295548-70295549	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs2736494	chr4:70295563-70295564	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs368892281	chr4:70295567-70295568	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs527512382	chr4:70295572-70295573	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs138236762	chr4:70295577-70295578	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs567254420	chr4:70295578-70295579	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs541160322	chr4:70295596-70295597	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs549454504	chr4:70295597-70295598	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs569355703	chr4:70295611-70295612	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs538222461	chr4:70295612-70295613	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs558064545	chr4:70295617-70295618	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs578170676	chr4:70295622-70295623	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs143708310	chr4:70295630-70295631	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs554294711	chr4:70295639-70295640	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs574144649	chr4:70295651-70295652	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs577620963	chr4:70295676-70295677	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs543191895	chr4:70295692-70295693	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs62307245	chr4:70295719-70295720	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs62307246	chr4:70295728-70295729	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs183740619	chr4:70295758-70295759	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs188724041	chr4:70295760-70295761	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs13117044	chr4:70295788-70295789	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs527536106	chr4:70295789-70295790	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs540880441	chr4:70295847-70295848	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs561176381	chr4:70295863-70295864	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs369168588	chr4:70295880-70295881	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs569393130	chr4:70295909-70295910	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs542923185	chr4:70295917-70295918	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs559549060	chr4:70295952-70295953	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Ovarian clear cell carcinoma	21343371	CNVD
Oral cancer	21386901	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:156 , 50 per page) page: 1 2 3 4

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

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