Variant report

Variant	nsv1013269
Chromosome Location	chr4:70044546-70120322
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:347)
CpG islands
(count:244)
Chromatin interactive
region (count:3)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70080605-70080753	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70105540-70105900	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70106482-70106878	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70047409-70047599	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:70105523-70105754	K562	blood:	n/a	n/a
6	ARID3A	chr4:70045525-70045926	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:70056442-70056604	HepG2	liver:	n/a	n/a
8	ATF1	chr4:70087666-70087866	K562	blood:	n/a	n/a
9	ATF1	chr4:70105493-70105808	K562	blood:	n/a	n/a
10	ATF1	chr4:70044510-70044858	K562	blood:	n/a	n/a
11	BACH1	chr4:70097393-70097475	K562	blood:	n/a	n/a
12	BCL3	chr4:70080358-70080837	A549	lung:	n/a	n/a
13	BHLHE40	chr4:70047447-70047661	HepG2	liver:	n/a	n/a
14	BHLHE40	chr4:70057696-70057810	K562	blood:	n/a	n/a
15	BHLHE40	chr4:70105574-70105707	K562	blood:	n/a	n/a
16	BHLHE40	chr4:70044628-70044869	K562	blood:	n/a	n/a
17	BHLHE40	chr4:70087582-70087589	K562	blood:	n/a	n/a
18	CCNT2	chr4:70105530-70105702	K562	blood:	n/a	n/a
19	CEBPB	chr4:70044638-70044861	K562	blood:	n/a	n/a
20	CEBPB	chr4:70106514-70106708	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:70105462-70105782	K562	blood:	n/a	n/a
22	CEBPB	chr4:70045536-70045885	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:70077980-70078075	K562	blood:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
24	CEBPB	chr4:70107648-70107863	HepG2	liver:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
25	CEBPB	chr4:70080509-70080873	A549	lung:	n/a	n/a
26	CEBPB	chr4:70047441-70047516	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:70044569-70044904	K562	blood:	n/a	n/a
28	CEBPB	chr4:70046596-70046924	HepG2	liver:	n/a	chr4:70046754-70046765 chr4:70046753-70046764
29	CEBPB	chr4:70077881-70078188	HepG2	liver:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
30	CEBPB	chr4:70077864-70078215	IMR90	lung:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
31	CEBPB	chr4:70118972-70119263	HepG2	liver:	n/a	chr4:70119163-70119176
32	CEBPB	chr4:70105548-70105721	K562	blood:	n/a	n/a
33	CEBPB	chr4:70059993-70060205	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:70045638-70045779	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:70107631-70107834	A549	lung:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
36	CEBPD	chr4:70045604-70045791	HepG2	liver:	n/a	n/a
37	CEBPD	chr4:70105414-70105831	K562	blood:	n/a	n/a
38	CEBPD	chr4:70044512-70044940	K562	blood:	n/a	n/a
39	CREB1	chr4:70045635-70045816	HepG2	liver:	n/a	n/a
40	CTCF	chr4:70089054-70089358	A549	lung:	n/a	n/a
41	CTCF	chr4:70097000-70097025	GM13977	blood:	n/a	n/a
42	CTCF	chr4:70089128-70089240	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr4:70089095-70089280	MCF-7	breast:	n/a	n/a
44	CTCF	chr4:70116415-70116447	Lung_OC	lung:	n/a	n/a
45	CTCF	chr4:70089071-70089282	HepG2	liver:	n/a	n/a
46	CTCF	chr4:70070599-70070664	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr4:70077161-70077220	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr4:70081934-70082033	GM10248	blood:	n/a	n/a
49	CTCF	chr4:70099241-70099301	GM10248	blood:	n/a	n/a
50	CTCF	chr4:70089049-70089337	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70065325-70065375	Caco-2	colon:	n/a
2	chr4:70065325-70065375	AoSMC	blood vessel:	n/a
3	chr4:70064835-70064885	Caco-2	colon:	n/a
4	chr4:70064835-70064885	HCF	heart:	n/a
5	chr4:70064835-70064885	AoSMC	blood vessel:	n/a
6	chr4:70066318-70066368	HepG2	liver:	n/a
7	chr4:70080453-70080503	GM12892	blood:	n/a
8	chr4:70065325-70065375	RPTEC	kidney:	n/a
9	chr4:70080453-70080503	U87	brain:	n/a
10	chr4:70066318-70066368	A549	lung:	n/a
11	chr4:70065325-70065375	HUVEC	blood vessel:	n/a
12	chr4:70064835-70064885	NH-A	brain:	n/a
13	chr4:70064835-70064885	NT2-D1	testis:	n/a
14	chr4:70065325-70065375	HEEpiC	esophagus:	n/a
15	chr4:70080453-70080503	ovcar-3	ovarian:	n/a
16	chr4:70080453-70080503	HCM	heart:	n/a
17	chr4:70080453-70080503	SK-N-SH_RA	brain:	n/a
18	chr4:70064835-70064885	HRCEpiC	kidney:	n/a
19	chr4:70065325-70065375	MCF-7	breast:	n/a
20	chr4:70066318-70066368	Jurkat	blood:	n/a
21	chr4:70080453-70080503	AG04450	lung:	fetal
22	chr4:70066318-70066368	GM12892	blood:	n/a
23	chr4:70065325-70065375	NH-A	brain:	n/a
24	chr4:70064835-70064885	GM06990	blood:	n/a
25	chr4:70065325-70065375	HCM	heart:	n/a
26	chr4:70064835-70064885	SK-N-MC	brain:	n/a
27	chr4:70080453-70080503	BJ	skin:	n/a
28	chr4:70065325-70065375	IMR90	lung:	fetal
29	chr4:70064835-70064885	BE2_C	brain:	n/a
30	chr4:70065325-70065375	MCF10A-Er-Src	breast:	n/a
31	chr4:70080453-70080503	SK-N-SH	brain:	n/a
32	chr4:70064835-70064885	IMR90	lung:	fetal
33	chr4:70066318-70066368	NH-A	brain:	n/a
34	chr4:70064835-70064885	GM19239	blood:	n/a
35	chr4:70080453-70080503	ECC-1	luminal epithelium:	n/a
36	chr4:70064835-70064885	GM12892	blood:	n/a
37	chr4:70064835-70064885	HEEpiC	esophagus:	n/a
38	chr4:70066318-70066368	CMK	blood:	n/a
39	chr4:70066318-70066368	Hela-S3	cervix:	n/a
40	chr4:70064835-70064885	AG04450	lung:	fetal
41	chr4:70066318-70066368	GM12878	blood:	n/a
42	chr4:70080453-70080503	MCF-7	breast:	n/a
43	chr4:70064835-70064885	LNCaP	prostate:	n/a
44	chr4:70065325-70065375	HMEC	breast:	n/a
45	chr4:70065325-70065375	HEK293	kidney:	embryo
46	chr4:70080453-70080503	HEEpiC	esophagus:	n/a
47	chr4:70066318-70066368	AG04450	lung:	fetal
48	chr4:70066318-70066368	RPTEC	kidney:	n/a
49	chr4:70064835-70064885	HepG2	liver:	n/a
50	chr4:70080453-70080503	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:
2	chr4:69673177..69674687-chr4:70085938..70087696,2	MCF-7	breast:
3	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-1	chr4:70047378-70048090	NONHSAT096756
2	lnc-UGT2B28-1	chr4:70066890-70067002	ENSG00000250696.1
3	lnc-UGT2B28-1	chr4:70080191-70082484	ENSG00000250696.1
4	lnc-UGT2B28-1	chr4:70047818-70048090	ENSG00000250696.1
5	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
6	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
7	lnc-UGT2B28-1	chr4:70061386-70061489	ENSG00000250696.1
8	lnc-UGT2B28-1	chr4:70066190-70066296	ENSG00000250696.1
9	lnc-UGT2B28-1	chr4:70080191-70080193	ENSG00000250696.1
10	lnc-UGT2B28-1	chr4:70066138-70066296	ENSG00000250696.1

No data

Variant related genes	Relation type
ENSG00000196472	TF binding region
ENSG00000250696	TF binding region
ENSG00000268803	TF binding region
ENSG00000249763	TF binding region
UGT2B11	TF binding region
ENSG00000196472	CpG island
ENSG00000250696	CpG island
ENSG00000268803	CpG island
ENSG00000249763	CpG island
UGT2B11	CpG island

Extended variants
information (count: 1994 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1994 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529215221	chr4:70044556-70044557	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs556706463	chr4:70044605-70044606	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs138130438	chr4:70044607-70044608	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs549123138	chr4:70044617-70044618	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs568962462	chr4:70044624-70044625	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs537912999	chr4:70044631-70044632	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs186478467	chr4:70044637-70044638	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs4318716	chr4:70044665-70044666	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs4318717	chr4:70044686-70044687	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs190915592	chr4:70044694-70044695	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs546229466	chr4:70044742-70044743	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs573442386	chr4:70044771-70044772	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs535776226	chr4:70044782-70044783	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs114841879	chr4:70044794-70044795	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs575447174	chr4:70044796-70044797	Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs544434647	chr4:70044826-70044827	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs564217232	chr4:70044864-70044865	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs142215715	chr4:70044878-70044879	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs549801765	chr4:70044886-70044887	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs553124692	chr4:70044903-70044904	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs373147554	chr4:70044904-70044905	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs540226973	chr4:70044908-70044909	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs74923404	chr4:70044913-70044914	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs180865832	chr4:70044917-70044918	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs115033222	chr4:70044940-70044941	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs562669867	chr4:70044999-70045000	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs531519109	chr4:70045000-70045001	Active TSS Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs576502489	chr4:70045033-70045034	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs186335899	chr4:70045037-70045038	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs551630701	chr4:70045061-70045062	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs386675657	chr4:70045065-70045066	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs4324612	chr4:70045066-70045067	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs191343958	chr4:70045069-70045070	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs567172459	chr4:70045082-70045083	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs536109592	chr4:70045083-70045084	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs562121997	chr4:70045093-70045094	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs534893199	chr4:70045107-70045108	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs113442421	chr4:70045116-70045117	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs187488283	chr4:70045132-70045133	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs538043662	chr4:70045138-70045139	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs557686539	chr4:70045205-70045206	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs557972703	chr4:70045207-70045208	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs199753313	chr4:70045211-70045212	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs374802562	chr4:70045228-70045229	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs577677865	chr4:70045274-70045275	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs140252384	chr4:70045283-70045284	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs190564097	chr4:70045336-70045337	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs573968347	chr4:70045349-70045350	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs559833184	chr4:70045361-70045362	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs57075079	chr4:70045368-70045369	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioblastoma multiforme	21510904	CNVD

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70043600-70044800	Enhancers	Fetal Intestine Small	intestine
2	chr4:70043600-70045600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:70043800-70044800	Weak transcription	Fetal Intestine Large	intestine
4	chr4:70044000-70044600	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr4:70044400-70044600	Enhancers	Liver	Liver
6	chr4:70044400-70045000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:70044400-70045400	Enhancers	Stomach Mucosa	stomach
8	chr4:70044600-70045000	Flanking Active TSS	Liver	Liver
9	chr4:70044800-70045000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:70044800-70045200	Enhancers	Primary B cells from peripheral blood	blood
11	chr4:70044800-70045400	Flanking Active TSS	Fetal Intestine Small	intestine
12	chr4:70044800-70045600	Enhancers	Fetal Intestine Large	intestine
13	chr4:70045000-70045200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:70045000-70045200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr4:70045000-70045600	Enhancers	Duodenum Mucosa	Duodenum
16	chr4:70045000-70045600	Enhancers	HepG2	liver
17	chr4:70045000-70045800	Enhancers	Primary hematopoietic stem cells	blood
18	chr4:70045000-70046200	Enhancers	Liver	Liver
19	chr4:70045200-70046200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:70045200-70047400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:70045400-70045600	Enhancers	Fetal Intestine Small	intestine
22	chr4:70045600-70046600	Weak transcription	HepG2	liver
23	chr4:70046200-70047400	Weak transcription	Liver	Liver
24	chr4:70046600-70046800	Enhancers	HepG2	liver
25	chr4:70046800-70047400	Weak transcription	HepG2	liver
26	chr4:70047200-70048000	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr4:70047400-70047600	Enhancers	Liver	Liver
28	chr4:70047400-70047600	Enhancers	HepG2	liver
29	chr4:70047400-70048000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr4:70056400-70057600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr4:70056400-70058400	Enhancers	HepG2	liver
32	chr4:70057400-70058000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:70057600-70057800	Enhancers	Liver	Liver
34	chr4:70058200-70058400	ZNF genes & repeats	Liver	Liver
35	chr4:70058400-70059000	Weak transcription	Liver	Liver
36	chr4:70059000-70059800	Enhancers	Liver	Liver
37	chr4:70059800-70060400	Enhancers	HepG2	liver
38	chr4:70059800-70066800	Weak transcription	Liver	Liver
39	chr4:70060000-70060400	Enhancers	Stomach Mucosa	stomach
40	chr4:70060000-70060800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:70062000-70063200	Enhancers	HMEC	breast
42	chr4:70062400-70063000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:70062600-70063400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:70066800-70067800	Strong transcription	Liver	Liver
45	chr4:70067800-70070600	Weak transcription	Liver	Liver
46	chr4:70076400-70076600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr4:70076800-70077800	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr4:70077800-70078200	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr4:70080400-70080800	Enhancers	HepG2	liver
50	chr4:70080600-70081200	Enhancers	Rectal Smooth Muscle	rectum

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