Variant report

Variant	nsv879389
Chromosome Location	chr4:70037747-70129929
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:353)
CpG islands
(count:244)
Chromatin interactive
region (count:3)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70056442-70056604	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70047409-70047599	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70080605-70080753	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70106482-70106878	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:70105540-70105900	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:70105523-70105754	K562	blood:	n/a	n/a
7	ARID3A	chr4:70045525-70045926	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	chr4:70105574-70105707	K562	blood:	n/a	n/a
14	BHLHE40	chr4:70047447-70047661	HepG2	liver:	n/a	n/a
15	BHLHE40	chr4:70057696-70057810	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	chr4:70046596-70046924	HepG2	liver:	n/a	chr4:70046754-70046765 chr4:70046753-70046764
20	CEBPB	chr4:70118972-70119263	HepG2	liver:	n/a	chr4:70119163-70119176
21	CEBPB	chr4:70044569-70044904	K562	blood:	n/a	n/a
22	CEBPB	chr4:70047441-70047516	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:70045536-70045885	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:70107648-70107863	HepG2	liver:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
25	CEBPB	chr4:70105462-70105782	K562	blood:	n/a	n/a
26	CEBPB	chr4:70077864-70078215	IMR90	lung:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
27	CEBPB	chr4:70107631-70107834	A549	lung:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
28	CEBPB	chr4:70106514-70106708	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:70045638-70045779	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:70077881-70078188	HepG2	liver:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
31	CEBPB	chr4:70077980-70078075	K562	blood:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
32	CEBPB	chr4:70059993-70060205	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:70080509-70080873	A549	lung:	n/a	n/a
34	CEBPB	chr4:70044638-70044861	K562	blood:	n/a	n/a
35	CEBPB	chr4:70105548-70105721	K562	blood:	n/a	n/a
36	CEBPD	chr4:70044512-70044940	K562	blood:	n/a	n/a
37	CEBPD	chr4:70105414-70105831	K562	blood:	n/a	n/a
38	CEBPD	chr4:70045604-70045791	HepG2	liver:	n/a	n/a
39	CREB1	chr4:70045635-70045816	HepG2	liver:	n/a	n/a
40	CTCF	chr4:70078196-70078250	GM13976	blood:	n/a	n/a
41	CTCF	chr4:70089126-70089248	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:70089054-70089358	A549	lung:	n/a	n/a
43	CTCF	chr4:70082912-70082994	GM10248	blood:	n/a	n/a
44	CTCF	chr4:70105505-70105507	LNCaP	prostate:	n/a	n/a
45	CTCF	chr4:70057643-70057792	Lung_OC	lung:	n/a	n/a
46	CTCF	chr4:70116866-70116969	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr4:70089131-70089152	Gliobla	brain:	n/a	n/a
48	CTCF	chr4:70089151-70089329	LNCaP	prostate:	n/a	n/a
49	CTCF	chr4:70109174-70109245	GM13976	blood:	n/a	n/a
50	CTCF	chr4:70089103-70089279	A549	lung:	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	CMK	blood:	n/a
2	chr4:70064835-70064885	AoSMC	blood vessel:	n/a
3	chr4:70066318-70066368	A549	lung:	n/a
4	chr4:70066318-70066368	GM12892	blood:	n/a
5	chr4:70066318-70066368	Caco-2	colon:	n/a
6	chr4:70064835-70064885	HCT-116	colon:	n/a
7	chr4:70066318-70066368	HNPCEpiC	eye:	n/a
8	chr4:70080453-70080503	LNCaP	prostate:	n/a
9	chr4:70065325-70065375	HEEpiC	esophagus:	n/a
10	chr4:70066318-70066368	SKMC	muscle:	n/a
11	chr4:70080453-70080503	ECC-1	luminal epithelium:	n/a
12	chr4:70066318-70066368	U87	brain:	n/a
13	chr4:70065325-70065375	HAEpiC	amniotic membrane:	n/a
14	chr4:70064835-70064885	HL-60	blood:	n/a
15	chr4:70066318-70066368	SK-N-MC	brain:	n/a
16	chr4:70065325-70065375	AG09319	gingival:	n/a
17	chr4:70065325-70065375	HCM	heart:	n/a
18	chr4:70066318-70066368	GM12878	blood:	n/a
19	chr4:70066318-70066368	GM12891	blood:	n/a
20	chr4:70064835-70064885	AG04450	lung:	fetal
21	chr4:70065325-70065375	HepG2	liver:	n/a
22	chr4:70065325-70065375	HL-60	blood:	n/a
23	chr4:70065325-70065375	K562	blood:	n/a
24	chr4:70064835-70064885	SK-N-MC	brain:	n/a
25	chr4:70080453-70080503	HUVEC	blood vessel:	n/a
26	chr4:70080453-70080503	NT2-D1	testis:	n/a
27	chr4:70080453-70080503	NHDF-neo	bronchial:	n/a
28	chr4:70064835-70064885	HMEC	breast:	n/a
29	chr4:70066318-70066368	Hela-S3	cervix:	n/a
30	chr4:70066318-70066368	AG09319	gingival:	n/a
31	chr4:70080453-70080503	HCF	heart:	n/a
32	chr4:70080453-70080503	HRCEpiC	kidney:	n/a
33	chr4:70080453-70080503	SK-N-MC	brain:	n/a
34	chr4:70080453-70080503	Hela-S3	cervix:	n/a
35	chr4:70066318-70066368	NB4	blood:	n/a
36	chr4:70065325-70065375	PrEC	prostate:	n/a
37	chr4:70066318-70066368	GM19239	blood:	n/a
38	chr4:70066318-70066368	AG04449	skin:	fetal
39	chr4:70064835-70064885	AG10803	skin:	n/a
40	chr4:70066318-70066368	HMEC	breast:	n/a
41	chr4:70080453-70080503	Caco-2	colon:	n/a
42	chr4:70065325-70065375	AG04450	lung:	fetal
43	chr4:70064835-70064885	MCF-7	breast:	n/a
44	chr4:70066318-70066368	AoSMC	blood vessel:	n/a
45	chr4:70064835-70064885	IMR90	lung:	fetal
46	chr4:70080453-70080503	MCF-7	breast:	n/a
47	chr4:70064835-70064885	NH-A	brain:	n/a
48	chr4:70066318-70066368	SK-N-SH_RA	brain:	n/a
49	chr4:70065325-70065375	HCPEpiC	choroid plexus:	n/a
50	chr4:70065325-70065375	AG10803	skin:	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	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:
3	chr4:69673177..69674687-chr4:70085938..70087696,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-1	chr4:70066190-70066296	ENSG00000250696.1
2	lnc-UGT2B28-1	chr4:70066890-70067002	ENSG00000250696.1
3	lnc-UGT2B28-1	chr4:70080191-70080193	ENSG00000250696.1
4	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
5	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
6	lnc-UGT2B28-1	chr4:70047378-70048090	NONHSAT096756
7	lnc-UGT2B28-1	chr4:70047818-70048090	ENSG00000250696.1
8	lnc-UGT2B28-1	chr4:70080191-70082484	ENSG00000250696.1
9	lnc-UGT2B28-1	chr4:70061386-70061489	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: 2414 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2414 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7671480	chr4:70037747-70037748	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571067396	chr4:70037768-70037769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538768357	chr4:70037772-70037773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529927080	chr4:70037802-70037803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550032587	chr4:70037804-70037805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569710076	chr4:70037814-70037815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572054923	chr4:70037834-70037835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538399515	chr4:70037838-70037839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552139761	chr4:70037864-70037865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565548500	chr4:70037875-70037876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552596483	chr4:70037883-70037884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4460076	chr4:70037892-70037893	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs373636751	chr4:70037951-70037952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538231119	chr4:70037988-70037989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147713978	chr4:70037996-70037997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188940182	chr4:70037997-70037998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575231508	chr4:70038051-70038052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141264931	chr4:70038073-70038074	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4273536	chr4:70038077-70038078	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs192256843	chr4:70038082-70038083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7658386	chr4:70038092-70038093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185386701	chr4:70038112-70038113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561148513	chr4:70038266-70038267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530041880	chr4:70038278-70038279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190684957	chr4:70038281-70038282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569204371	chr4:70038299-70038300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs4463130	chr4:70038345-70038346	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs369704394	chr4:70038355-70038356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577466688	chr4:70038370-70038371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs180816407	chr4:70038386-70038387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186259304	chr4:70038401-70038402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565642167	chr4:70038407-70038408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188452535	chr4:70038445-70038446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547810365	chr4:70038451-70038452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567617354	chr4:70038471-70038472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536589423	chr4:70038477-70038478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549043575	chr4:70038494-70038495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181301700	chr4:70038497-70038498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539097844	chr4:70038569-70038570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567528319	chr4:70038595-70038596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs61383951	chr4:70038640-70038641	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs57775540	chr4:70038658-70038659	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs370166662	chr4:70038662-70038663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574772470	chr4:70038686-70038687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543360264	chr4:70038694-70038695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185530277	chr4:70038722-70038723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553167107	chr4:70038725-70038726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs199622555	chr4:70038731-70038732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545848953	chr4:70038738-70038739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190382385	chr4:70038741-70038742	Enhancers Weak transcription	n/a	n/a	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
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:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70035200-70043600	Weak transcription	Fetal Intestine Small	intestine
2	chr4:70035800-70038200	Enhancers	Liver	Liver
3	chr4:70038200-70038600	Weak transcription	Liver	Liver
4	chr4:70038600-70038800	Enhancers	Liver	Liver
5	chr4:70038800-70041000	Weak transcription	Liver	Liver
6	chr4:70041000-70042000	Strong transcription	Liver	Liver
7	chr4:70042000-70044400	Weak transcription	Liver	Liver
8	chr4:70043600-70043800	Enhancers	Fetal Intestine Large	intestine
9	chr4:70043600-70044800	Enhancers	Fetal Intestine Small	intestine
10	chr4:70043600-70045600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr4:70043800-70044800	Weak transcription	Fetal Intestine Large	intestine
12	chr4:70044000-70044600	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr4:70044200-70044400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr4:70044400-70044600	Enhancers	Liver	Liver
15	chr4:70044400-70045000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr4:70044400-70045400	Enhancers	Stomach Mucosa	stomach
17	chr4:70044600-70045000	Flanking Active TSS	Liver	Liver
18	chr4:70044800-70045000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:70044800-70045200	Enhancers	Primary B cells from peripheral blood	blood
20	chr4:70044800-70045400	Flanking Active TSS	Fetal Intestine Small	intestine
21	chr4:70044800-70045600	Enhancers	Fetal Intestine Large	intestine
22	chr4:70045000-70045200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:70045000-70045200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr4:70045000-70045600	Enhancers	Duodenum Mucosa	Duodenum
25	chr4:70045000-70045600	Enhancers	HepG2	liver
26	chr4:70045000-70045800	Enhancers	Primary hematopoietic stem cells	blood
27	chr4:70045000-70046200	Enhancers	Liver	Liver
28	chr4:70045200-70046200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:70045200-70047400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr4:70045400-70045600	Enhancers	Fetal Intestine Small	intestine
31	chr4:70045600-70046600	Weak transcription	HepG2	liver
32	chr4:70046200-70047400	Weak transcription	Liver	Liver
33	chr4:70046600-70046800	Enhancers	HepG2	liver
34	chr4:70046800-70047400	Weak transcription	HepG2	liver
35	chr4:70047200-70048000	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr4:70047400-70047600	Enhancers	Liver	Liver
37	chr4:70047400-70047600	Enhancers	HepG2	liver
38	chr4:70047400-70048000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr4:70056400-70057600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr4:70056400-70058400	Enhancers	HepG2	liver
41	chr4:70057400-70058000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:70057600-70057800	Enhancers	Liver	Liver
43	chr4:70058200-70058400	ZNF genes & repeats	Liver	Liver
44	chr4:70058400-70059000	Weak transcription	Liver	Liver
45	chr4:70059000-70059800	Enhancers	Liver	Liver
46	chr4:70059800-70060400	Enhancers	HepG2	liver
47	chr4:70059800-70066800	Weak transcription	Liver	Liver
48	chr4:70060000-70060400	Enhancers	Stomach Mucosa	stomach
49	chr4:70060000-70060800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:70062000-70063200	Enhancers	HMEC	breast

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