Variant report

Variant	esv2757035
Chromosome Location	chr4:10051761-10064004
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:70)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:70 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:10052855-10053185	HepG2	liver:	n/a	chr4:10053009-10053020
2	CEBPB	chr4:10055775-10055917	HepG2	liver:	n/a	chr4:10055872-10055883
3	CEBPB	chr4:10063339-10063704	IMR90	lung:	n/a	chr4:10063514-10063525
4	CEBPB	chr4:10052889-10053146	A549	lung:	n/a	chr4:10053009-10053020
5	CEBPB	chr4:10055701-10056034	HepG2	liver:	n/a	chr4:10055872-10055883
6	CEBPB	chr4:10063381-10063653	HepG2	liver:	n/a	chr4:10063514-10063525
7	CEBPB	chr4:10052869-10053177	IMR90	lung:	n/a	chr4:10053009-10053020
8	CEBPB	chr4:10052999-10053012	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr4:10054920-10054983	K562	blood:	n/a	n/a
10	CTCF	chr4:10054900-10055050	NHEK	skin:	n/a	n/a
11	CTCF	chr4:10063000-10063150	AG04449	skin:	n/a	n/a
12	CTCF	chr4:10054920-10055070	HepG2	liver:	n/a	n/a
13	E2F4	chr4:10063383-10063646	MCF10A-Er-Src	breast:	n/a	n/a
14	E2F4	chr4:10056046-10056224	MCF10A-Er-Src	breast:	n/a	chr4:10056156-10056170
15	ELK1	chr4:10058936-10058952	K562	blood:	n/a	n/a
16	EP300	chr4:10055749-10055925	HepG2	liver:	n/a	chr4:10055911-10055921
17	FOS	chr4:10063284-10063672	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr4:10063294-10063696	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr4:10063298-10063659	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr4:10063329-10063667	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr4:10056233-10056261	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr4:10056334-10056654	MCF10A-Er-Src	breast:	n/a	chr4:10056565-10056574 chr4:10056451-10056459
23	FOXA2	chr4:10055735-10056015	HepG2	liver:	n/a	chr4:10055908-10055920
24	FOXP2	chr4:10056364-10056580	PFSK-1	brain:	n/a	n/a
25	GATA2	chr4:10052736-10053119	HUVEC	blood vessel:	n/a	chr4:10052882-10052896
26	GTF2F1	chr4:10055736-10055810	H1-hESC	embryonic stem cell:	n/a	n/a
27	HNF4A	chr4:10055784-10056015	HepG2	liver:	n/a	n/a
28	HNF4G	chr4:10058035-10058263	HepG2	liver:	n/a	chr4:10058154-10058169
29	JUND	chr4:10052582-10052646	HepG2	liver:	n/a	n/a
30	MAFK	chr4:10063701-10064001	IMR90	lung:	n/a	chr4:10063858-10063873
31	MAFK	chr4:10063712-10064035	HepG2	liver:	n/a	chr4:10063858-10063873
32	MAFK	chr4:10063757-10064023	HepG2	liver:	n/a	chr4:10063858-10063873
33	MAX	chr4:10055581-10056159	HepG2	liver:	n/a	chr4:10055867-10055876 chr4:10055869-10055876
34	MAX	chr4:10055768-10055886	HepG2	liver:	n/a	chr4:10055867-10055876 chr4:10055869-10055876
35	MAX	chr4:10055637-10056036	HepG2	liver:	n/a	chr4:10055867-10055876 chr4:10055869-10055876
36	MXI1	chr4:10055678-10055944	HepG2	liver:	n/a	chr4:10055866-10055875
37	MYC	chr4:10058745-10058779	NB4	blood:	n/a	n/a
38	MYC	chr4:10063378-10063670	MCF10A-Er-Src	breast:	n/a	n/a
39	MYC	chr4:10055831-10055893	HepG2	liver:	n/a	chr4:10055867-10055876 chr4:10055869-10055876
40	NFIC	chr4:10056004-10056500	ECC-1	luminal epithelium:	n/a	n/a
41	POLR2A	chr4:10063384-10063587	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr4:10062516-10062542	HepG2	liver:	n/a	n/a
43	POLR2A	chr4:10062924-10062956	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr4:10060124-10062051	K562	blood:	n/a	n/a
45	POLR2A	chr4:10053454-10053467	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr4:10055801-10056055	K562	blood:	n/a	n/a
47	POLR2A	chr4:10063356-10064250	K562	blood:	n/a	n/a
48	POLR2A	chr4:10052203-10053090	K562	blood:	n/a	n/a
49	POLR2A	chr4:10062486-10064107	IMR90	lung:	n/a	n/a
50	POLR2A	chr4:10062391-10063119	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10052335-10052385	HUVEC	blood vessel:	n/a
2	chr4:10052335-10052385	NHDF-neo	bronchial:	n/a
3	chr4:10052335-10052385	HRE	kidney:	n/a
4	chr4:10052335-10052385	HCT-116	colon:	n/a
5	chr4:10052335-10052385	GM12892	blood:	n/a
6	chr4:10052335-10052385	PrEC	prostate:	n/a
7	chr4:10052335-10052385	SAEC	small airway:	n/a
8	chr4:10052335-10052385	AoSMC	blood vessel:	n/a
9	chr4:10052335-10052385	BJ	skin:	n/a
10	chr4:10052335-10052385	GM06990	blood:	n/a
11	chr4:10052335-10052385	HIPEpiC	eye:	n/a
12	chr4:10052335-10052385	SKMC	muscle:	n/a
13	chr4:10052335-10052385	SK-N-SH	brain:	n/a
14	chr4:10052335-10052385	AG09309	skin:	n/a
15	chr4:10052335-10052385	SK-N-SH_RA	brain:	n/a
16	chr4:10052335-10052385	NHBE	bronchial:	n/a
17	chr4:10052335-10052385	A549	lung:	n/a
18	chr4:10052335-10052385	HRCEpiC	kidney:	n/a
19	chr4:10052335-10052385	HCPEpiC	choroid plexus:	n/a
20	chr4:10052335-10052385	PFSK-1	brain:	n/a
21	chr4:10052335-10052385	MCF-7	breast:	n/a
22	chr4:10052335-10052385	AG04450	lung:	fetal
23	chr4:10052335-10052385	HCM	heart:	n/a
24	chr4:10052335-10052385	T-47D	breast:	n/a
25	chr4:10052335-10052385	ovcar-3	ovarian:	n/a
26	chr4:10052335-10052385	HNPCEpiC	eye:	n/a
27	chr4:10052335-10052385	HepG2	liver:	n/a
28	chr4:10052335-10052385	HCF	heart:	n/a
29	chr4:10052335-10052385	AG09319	gingival:	n/a
30	chr4:10052335-10052385	SK-N-MC	brain:	n/a
31	chr4:10052335-10052385	Caco-2	colon:	n/a
32	chr4:10052335-10052385	Jurkat	blood:	n/a
33	chr4:10052335-10052385	AG10803	skin:	n/a
34	chr4:10052335-10052385	IMR90	lung:	fetal
35	chr4:10052335-10052385	HEEpiC	esophagus:	n/a
36	chr4:10052335-10052385	Hela-S3	cervix:	n/a
37	chr4:10052335-10052385	PANC-1	pancreas:	n/a
38	chr4:10052335-10052385	GM12891	blood:	n/a
39	chr4:10052335-10052385	HEK293	kidney:	embryo
40	chr4:10052335-10052385	HPAEpiC	pulmonary alveolar:	n/a
41	chr4:10052335-10052385	RPTEC	kidney:	n/a
42	chr4:10052335-10052385	U87	brain:	n/a
43	chr4:10052335-10052385	HL-60	blood:	n/a
44	chr4:10052335-10052385	HMEC	breast:	n/a
45	chr4:10052335-10052385	HAEpiC	amniotic membrane:	n/a
46	chr4:10052335-10052385	LNCaP	prostate:	n/a
47	chr4:10052335-10052385	K562	blood:	n/a
48	chr4:10052335-10052385	ProgFib	skin:	n/a
49	chr4:10052335-10052385	BE2_C	brain:	n/a
50	chr4:10052335-10052385	NB4	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:10061810..10065204-chr4:10068602..10071736,4	MCF-7	breast:
2	chr4:10050227..10052553-chr4:10054498..10056882,2	K562	blood:
3	chr4:10063533..10065556-chr4:10116961..10119928,2	K562	blood:
4	chr4:10053096..10055486-chr4:10058375..10060110,2	K562	blood:
5	chr4:10008558..10010473-chr4:10063451..10065782,2	MCF-7	breast:
6	chr4:10060964..10064937-chr4:10066932..10071092,4	K562	blood:
7	chr4:10053096..10055486-chr4:10058375..10060110,2	K562	blood:

No data

Variant related genes	Relation type
SLC2A9	TF binding region
SLC2A9	CpG island
ENSG00000109667	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000223086	chromatin interactions

Extended variants
information (count: 556 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12499734	chr4:10051761-10051762	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529011428	chr4:10051798-10051799	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs77165435	chr4:10051846-10051847	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs117443909	chr4:10051860-10051861	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs114566282	chr4:10051864-10051865	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs117657217	chr4:10051878-10051879	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs560363002	chr4:10051881-10051882	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs78319160	chr4:10051944-10051945	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544428238	chr4:10052055-10052056	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs548748448	chr4:10052059-10052060	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs563749650	chr4:10052084-10052085	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs76381199	chr4:10052097-10052098	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs10939672	chr4:10052136-10052137	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs569259214	chr4:10052149-10052150	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs74947456	chr4:10052194-10052195	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs114450939	chr4:10052206-10052207	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs567131146	chr4:10052212-10052213	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs534258161	chr4:10052219-10052220	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs555987673	chr4:10052224-10052225	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs113921618	chr4:10052272-10052273	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs574331654	chr4:10052279-10052280	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs12650722	chr4:10052314-10052315	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs544823864	chr4:10052344-10052345	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs184033916	chr4:10052355-10052356	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577681391	chr4:10052413-10052414	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs370260868	chr4:10052420-10052421	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs139057978	chr4:10052433-10052434	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs143484897	chr4:10052434-10052435	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs373673353	chr4:10052446-10052447	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs147171965	chr4:10052455-10052456	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs560849598	chr4:10052462-10052463	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs531360488	chr4:10052507-10052508	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs75604947	chr4:10052521-10052522	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs6821843	chr4:10052528-10052529	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs533292571	chr4:10052535-10052536	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs551735954	chr4:10052536-10052537	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs370403911	chr4:10052560-10052561	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs528493739	chr4:10052566-10052567	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs6822023	chr4:10052594-10052595	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs534492887	chr4:10052605-10052606	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs6837659	chr4:10052610-10052611	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs567971105	chr4:10052629-10052630	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs187371120	chr4:10052641-10052642	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs190329601	chr4:10052650-10052651	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs528872618	chr4:10052694-10052695	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs544814109	chr4:10052712-10052713	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs182571761	chr4:10052728-10052729	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs550964747	chr4:10052765-10052766	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs111918489	chr4:10052812-10052813	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs116607976	chr4:10052817-10052818	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:266 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10035200-10065600	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr4:10035400-10065200	Weak transcription	Right Ventricle	heart
3	chr4:10035800-10068400	Weak transcription	Aorta	Aorta
4	chr4:10037000-10052400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:10037000-10056000	Weak transcription	Brain Cingulate Gyrus	brain
6	chr4:10041000-10065000	Weak transcription	Stomach Smooth Muscle	stomach
7	chr4:10044600-10064800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr4:10044800-10056800	Weak transcription	Psoas Muscle	Psoas
9	chr4:10044800-10058800	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr4:10046800-10051800	Enhancers	Fetal Intestine Small	intestine
11	chr4:10046800-10053600	Enhancers	Fetal Intestine Large	intestine
12	chr4:10048200-10065400	Weak transcription	Primary B cells from peripheral blood	blood
13	chr4:10049800-10052400	Enhancers	NHEK	skin
14	chr4:10049800-10052600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:10049800-10053400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:10049800-10054200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:10050000-10052000	Enhancers	Right Atrium	heart
18	chr4:10050000-10052400	Enhancers	HMEC	breast
19	chr4:10050000-10052600	Enhancers	Pancreas	Pancrea
20	chr4:10050000-10053600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:10050000-10065000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr4:10050000-10066400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr4:10050200-10052000	Enhancers	HepG2	liver
24	chr4:10050200-10054800	Weak transcription	Left Ventricle	heart
25	chr4:10050200-10062600	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr4:10050400-10053400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr4:10050400-10063000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr4:10050600-10052200	Weak transcription	Placenta	Placenta
29	chr4:10050600-10053200	Strong transcription	Primary T cells from cord blood	blood
30	chr4:10050800-10052600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr4:10050800-10053200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:10050800-10053600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr4:10051000-10052200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:10051000-10052600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr4:10051000-10053000	Enhancers	Esophagus	oesophagus
36	chr4:10051000-10053600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:10051000-10068200	Weak transcription	Duodenum Mucosa	Duodenum
38	chr4:10051200-10052800	Weak transcription	Fetal Heart	heart
39	chr4:10051200-10053200	Enhancers	Thymus	Thymus
40	chr4:10051200-10057600	Weak transcription	Primary B cells from cord blood	blood
41	chr4:10051400-10052600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr4:10051400-10052800	Enhancers	Fetal Thymus	thymus
43	chr4:10051400-10053600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:10051400-10060400	Weak transcription	Spleen	Spleen
45	chr4:10051400-10076200	Weak transcription	Small Intestine	intestine
46	chr4:10051600-10052600	Enhancers	H9 Cell Line	embryonic stem cell
47	chr4:10051600-10052600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr4:10051600-10053200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr4:10051600-10053200	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr4:10051600-10053200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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