Variant report

Variant	esv1797624
Chromosome Location	chr4:8254784-8271983
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:8268932-8269253	K562	blood:	n/a	n/a
2	ATF1	chr4:8254361-8254786	K562	blood:	n/a	n/a
3	BHLHE40	chr4:8260314-8260592	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:8260365-8260601	K562	blood:	n/a	n/a
5	BHLHE40	chr4:8265162-8265446	K562	blood:	n/a	n/a
6	BHLHE40	chr4:8254185-8254854	K562	blood:	n/a	n/a
7	BHLHE40	chr4:8265116-8265491	HepG2	liver:	n/a	n/a
8	BHLHE40	chr4:8268745-8269240	K562	blood:	n/a	chr4:8269078-8269094
9	BRCA1	chr4:8269017-8269224	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr4:8268932-8269205	HepG2	liver:	n/a	n/a
11	CCNT2	chr4:8268882-8269163	K562	blood:	n/a	chr4:8269023-8269032
12	CCNT2	chr4:8254130-8254835	K562	blood:	n/a	n/a
13	CEBPB	chr4:8262340-8262694	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr4:8257720-8258031	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:8264842-8265226	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr4:8264878-8265137	A549	lung:	n/a	n/a
17	CEBPB	chr4:8262316-8262879	IMR90	lung:	n/a	n/a
18	CEBPB	chr4:8264859-8265179	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:8262458-8262588	A549	lung:	n/a	n/a
20	CEBPB	chr4:8264843-8265192	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:8265027-8265028	K562	blood:	n/a	n/a
22	CEBPD	chr4:8254373-8254819	K562	blood:	n/a	n/a
23	CHD2	chr4:8269076-8269258	K562	blood:	n/a	n/a
24	CHD2	chr4:8254492-8254791	K562	blood:	n/a	n/a
25	CHD2	chr4:8269075-8269158	HepG2	liver:	n/a	n/a
26	CHD2	chr4:8262444-8262643	Hela-S3	cervix:	n/a	n/a
27	CREB1	chr4:8271379-8271648	A549	lung:	n/a	n/a
28	CTBP2	chr4:8271453-8272043	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr4:8262520-8262670	AG10803	skin:	n/a	chr4:8262612-8262621
30	CTCF	chr4:8269000-8269150	Caco-2	colon:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
31	CTCF	chr4:8269000-8269150	HPAF	blood vessel:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
32	CTCF	chr4:8269000-8269150	AG04449	skin:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
33	CTCF	chr4:8268980-8269130	HCPEpiC	choroid plexus:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
34	CTCF	chr4:8269020-8269170	BE2_C	brain:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
35	CTCF	chr4:8262640-8262790	WI-38	lung:	n/a	n/a
36	CTCF	chr4:8268999-8269225	T-47D	breast:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
37	CTCF	chr4:8262520-8262670	AG04450	lung:	n/a	chr4:8262612-8262621
38	CTCF	chr4:8268902-8269238	K562	blood:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
39	CTCF	chr4:8263660-8263810	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr4:8268953-8269222	MCF-7	breast:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
41	CTCF	chr4:8268946-8269278	HepG2	liver:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
42	CTCF	chr4:8268962-8269197	HepG2	liver:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
43	CTCF	chr4:8269040-8269190	HCT-116	colon:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
44	CTCF	chr4:8268970-8269187	Spleen_OC	spleen:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
45	CTCF	chr4:8268960-8269110	MCF-7	breast:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
46	CTCF	chr4:8268980-8269130	MCF-7	breast:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
47	CTCF	chr4:8263760-8263910	HEK293	kidney:	n/a	n/a
48	CTCF	chr4:8269020-8269170	GM12871	blood:	n/a	chr4:8269082-8269092 chr4:8269077-8269095 chr4:8269078-8269094 chr4:8269080-8269093
49	CTCF	chr4:8268940-8269090	HFF	foreskin:	n/a	n/a
50	CTCF	chr4:8262480-8262630	HPF	lung:	n/a	chr4:8262612-8262621

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8263007-8263057	BE2_C	brain:	n/a
2	chr4:8263073-8263123	MCF10A-Er-Src	breast:	n/a
3	chr4:8271414-8271464	ovcar-3	ovarian:	n/a
4	chr4:8262659-8262709	T-47D	breast:	n/a
5	chr4:8263007-8263057	BE2_C	brain:	n/a
6	chr4:8263073-8263123	MCF10A-Er-Src	breast:	n/a
7	chr4:8271414-8271464	ovcar-3	ovarian:	n/a
8	chr4:8262659-8262709	T-47D	breast:	n/a
9	chr4:8271319-8271369	HIPEpiC	eye:	n/a
10	chr4:8271319-8271369	ovcar-3	ovarian:	n/a
11	chr4:8271319-8271369	HCT-116	colon:	n/a
12	chr4:8271414-8271464	PrEC	prostate:	n/a
13	chr4:8263073-8263123	Jurkat	blood:	n/a
14	chr4:8263007-8263057	Hepatocyte	liver:	n/a
15	chr4:8271236-8271286	SK-N-SH_RA	brain:	n/a
16	chr4:8262942-8262992	MCF-7	breast:	n/a
17	chr4:8271236-8271286	PrEC	prostate:	n/a
18	chr4:8271369-8271419	HUVEC	blood vessel:	n/a
19	chr4:8271236-8271286	AG10803	skin:	n/a
20	chr4:8271414-8271464	CMK	blood:	n/a
21	chr4:8262659-8262709	HepG2	liver:	n/a
22	chr4:8271507-8271557	HRPEpiC	eye:	n/a
23	chr4:8271414-8271464	SAEC	small airway:	n/a
24	chr4:8271507-8271557	BJ	skin:	n/a
25	chr4:8262589-8262639	SAEC	small airway:	n/a
26	chr4:8271369-8271419	PANC-1	pancreas:	n/a
27	chr4:8270184-8270234	PFSK-1	brain:	n/a
28	chr4:8271792-8271842	T-47D	breast:	n/a
29	chr4:8271236-8271286	AG04450	lung:	fetal
30	chr4:8271391-8271441	MCF10A-Er-Src	breast:	n/a
31	chr4:8271369-8271419	H1-hESC	embryonic stem cell:	embryo
32	chr4:8256315-8256365	NT2-D1	testis:	n/a
33	chr4:8268962-8269012	T-47D	breast:	n/a
34	chr4:8271196-8271246	HCF	heart:	n/a
35	chr4:8268962-8269012	AoSMC	blood vessel:	n/a
36	chr4:8256315-8256365	SK-N-SH	brain:	n/a
37	chr4:8262589-8262639	SK-N-SH	brain:	n/a
38	chr4:8262589-8262639	AG04450	lung:	fetal
39	chr4:8271236-8271286	HCT-116	colon:	n/a
40	chr4:8271196-8271246	SK-N-SH_RA	brain:	n/a
41	chr4:8262942-8262992	AG04450	lung:	fetal
42	chr4:8263007-8263057	NH-A	brain:	n/a
43	chr4:8262688-8262738	HCF	heart:	n/a
44	chr4:8262659-8262709	ovcar-3	ovarian:	n/a
45	chr4:8271319-8271369	HepG2	liver:	n/a
46	chr4:8271414-8271464	AG04450	lung:	fetal
47	chr4:8271391-8271441	ECC-1	luminal epithelium:	n/a
48	chr4:8271792-8271842	NHDF-neo	bronchial:	n/a
49	chr4:8256393-8256443	PrEC	prostate:	n/a
50	chr4:8270184-8270234	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:8268867..8271118-chr4:8273119..8275755,2	MCF-7	breast:
2	chr3:128902200..128903075-chr4:8271389..8271937,2	NB4	blood:
3	chr4:8261537..8264221-chr4:8264274..8265849,2	MCF-7	breast:
4	chr4:8261537..8264221-chr4:8264274..8265849,2	MCF-7	breast:
5	chr4:8244003..8244602-chr4:8267775..8268462,2	MCF-7	breast:
6	chr16:28834863..28835527-chr4:8271061..8271579,2	NB4	blood:
7	chr4:8268593..8269552-chr4:8403907..8405561,11	MCF-7	breast:
8	chr10:105156345..105156947-chr4:8271069..8272007,2	NB4	blood:
9	chr4:8254660..8257385-chr4:8260489..8263167,2	MCF-7	breast:
10	chr4:8252135..8255007-chr4:8262927..8264616,3	K562	blood:
11	chr4:8268620..8269557-chr4:8404343..8405485,5	K562	blood:
12	chr4:8252135..8254748-chr4:8262223..8264616,3	K562	blood:
13	chr4:8261913..8264810-chr4:8267913..8270603,2	K562	blood:
14	chr4:8268637..8269538-chr4:8412094..8412713,3	MCF-7	breast:
15	chr4:8271058..8271580-chr5:74632260..74632932,2	NB4	blood:
16	chr4:8263022..8264524-chr4:8271054..8272671,2	MCF-7	breast:
17	chr4:8252135..8255007-chr4:8262927..8264616,3	K562	blood:
18	chr4:8261994..8265646-chr4:8266271..8270310,6	MCF-7	breast:
19	chr4:8268685..8271204-chr4:8420095..8422355,2	MCF-7	breast:
20	chr4:8238966..8241301-chr4:8261569..8263591,2	MCF-7	breast:
21	chr4:8243618..8244524-chr4:8268726..8269548,3	MCF-7	breast:
22	chr4:8252940..8255402-chr4:8411571..8414054,2	K562	blood:
23	chr4:8254660..8257385-chr4:8260489..8263167,2	MCF-7	breast:
24	chr4:8266213..8269192-chr4:8274192..8276756,2	K562	blood:
25	chr4:8261994..8265646-chr4:8266271..8270310,6	MCF-7	breast:
26	chr4:8268241..8269567-chr4:8404622..8405485,4	MCF-7	breast:
27	chr4:8242105..8244343-chr4:8260959..8263973,3	MCF-7	breast:
28	chr4:8262200..8264510-chr4:8428848..8430829,2	MCF-7	breast:
29	chr4:8261913..8264810-chr4:8267913..8270603,2	K562	blood:
30	chr4:8271372..8272005-chr5:137514142..137514696,2	NB4	blood:

Variant related genes	Relation type
HTRA3	TF binding region
HTRA3	CpG island
ENSG00000112983	chromatin interactions
ENSG00000247372	chromatin interactions
ENSG00000148843	chromatin interactions
ENSG00000169714	chromatin interactions
ENSG00000112984	chromatin interactions
ENSG00000170801	chromatin interactions
ENSG00000125089	chromatin interactions
ENSG00000168488	chromatin interactions
ENSG00000087008	chromatin interactions

Extended variants
information (count: 842 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:842 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1678336	chr4:8254784-8254785	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527482596	chr4:8254786-8254787	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112119054	chr4:8254792-8254793	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187724941	chr4:8254848-8254849	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs192340977	chr4:8254918-8254919	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs140067333	chr4:8254953-8254954	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs549828985	chr4:8254958-8254959	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs571242187	chr4:8254979-8254980	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs538321019	chr4:8254985-8254986	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs184675930	chr4:8255006-8255007	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs566094163	chr4:8255066-8255067	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs536494484	chr4:8255083-8255084	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs554834135	chr4:8255098-8255099	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs1678335	chr4:8255104-8255105	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs537028271	chr4:8255126-8255127	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs116348938	chr4:8255127-8255128	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs577186784	chr4:8255135-8255136	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs541128170	chr4:8255147-8255148	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs370084596	chr4:8255167-8255168	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs530843573	chr4:8255202-8255203	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs115723336	chr4:8255212-8255213	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs542876127	chr4:8255258-8255259	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs549061276	chr4:8255320-8255321	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs188742505	chr4:8255367-8255368	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs373930146	chr4:8255378-8255379	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs543679759	chr4:8255391-8255392	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs116029666	chr4:8255423-8255424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs59269679	chr4:8255450-8255451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs397954496	chr4:8255459-8255460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200367425	chr4:8255460-8255461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201186906	chr4:8255461-8255462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550436325	chr4:8255510-8255511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571965257	chr4:8255515-8255516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144946243	chr4:8255537-8255538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192643276	chr4:8255553-8255554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565808758	chr4:8255576-8255577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530217300	chr4:8255612-8255613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372632198	chr4:8255613-8255614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10755198	chr4:8255674-8255675	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs184263434	chr4:8255720-8255721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188998727	chr4:8255771-8255772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115067850	chr4:8255781-8255782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114106001	chr4:8255820-8255821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535056128	chr4:8255825-8255826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553174761	chr4:8255832-8255833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575012029	chr4:8255835-8255836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370573479	chr4:8255857-8255858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554769949	chr4:8255882-8255883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567702306	chr4:8255888-8255889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs6837910	chr4:8255952-8255953	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:56)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
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
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
small cell lung cancer	20016488	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
Urothelial carcinoma	21177765	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Oligozoospermia	20877625	CNVD
Breast cancer	22522925	CNVD
Autism	20841430	CNVD

Chromatin state (count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8245000-8255800	Weak transcription	HMEC	breast
2	chr4:8245200-8255200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:8249800-8257200	Weak transcription	HSMM	muscle
4	chr4:8249800-8268400	Weak transcription	Right Atrium	heart
5	chr4:8249800-8268600	Weak transcription	Fetal Intestine Small	intestine
6	chr4:8250000-8257600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr4:8250600-8261800	Weak transcription	A549	lung
8	chr4:8253000-8256000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:8253200-8256200	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr4:8253200-8256800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:8253400-8257600	Weak transcription	Adipose Nuclei	Adipose
12	chr4:8253600-8256400	Enhancers	Placenta	Placenta
13	chr4:8253600-8257400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:8254000-8255200	Enhancers	K562	blood
15	chr4:8254200-8254800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:8254200-8255000	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr4:8254200-8255200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr4:8254200-8255200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr4:8254200-8255400	Bivalent Enhancer	HepG2	liver
20	chr4:8254200-8256000	Enhancers	Primary hematopoietic stem cells	blood
21	chr4:8254400-8254800	Enhancers	Fetal Lung	lung
22	chr4:8254400-8254800	Enhancers	Gastric	stomach
23	chr4:8254400-8254800	Enhancers	Placenta Amnion	Placenta Amnion
24	chr4:8254400-8255000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:8254400-8255200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:8254400-8255200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:8254400-8255400	Enhancers	Fetal Thymus	thymus
28	chr4:8254600-8254800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
29	chr4:8254600-8258000	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr4:8254800-8259000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr4:8254800-8271600	Weak transcription	Gastric	stomach
32	chr4:8255000-8255200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr4:8255000-8261800	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr4:8255200-8256400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:8255200-8259600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr4:8255200-8259600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr4:8255400-8255800	Weak transcription	Fetal Thymus	thymus
38	chr4:8255800-8256000	Enhancers	Fetal Thymus	thymus
39	chr4:8255800-8256200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:8255800-8256200	Enhancers	Esophagus	oesophagus
41	chr4:8255800-8256400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr4:8255800-8256400	Enhancers	NHEK	skin
43	chr4:8255800-8256600	Enhancers	HMEC	breast
44	chr4:8256000-8256200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:8256000-8259600	Weak transcription	Primary hematopoietic stem cells	blood
46	chr4:8256000-8260400	Weak transcription	Fetal Thymus	thymus
47	chr4:8256000-8264800	Enhancers	Fetal Muscle Leg	muscle
48	chr4:8256200-8257600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr4:8256200-8257600	Weak transcription	Esophagus	oesophagus
50	chr4:8256200-8257800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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