Variant report

Variant	esv1795061
Chromosome Location	chr4:69287209-69503681
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	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
6	BACH1	chr4:69318318-69318341	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:69316907-69317183	H1-hESC	embryonic stem cell:	n/a	chr4:69317106-69317120
8	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
9	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
10	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
11	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:69305163-69305286	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
15	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
16	CCNT2	chr4:69328625-69328750	K562	blood:	n/a	n/a
17	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:69300096-69300253	H1-hESC	embryonic stem cell:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
19	CEBPB	chr4:69321591-69322194	MCF-7	breast:	n/a	n/a
20	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:69308568-69308582	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:69321712-69322175	MCF-7	breast:	n/a	n/a
23	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
24	CEBPB	chr4:69300033-69300365	HepG2	liver:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
25	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
26	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
27	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:69300028-69300381	IMR90	lung:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
29	CEBPB	chr4:69327525-69327817	MCF-7	breast:	n/a	n/a
30	CEBPB	chr4:69312976-69313282	MCF-7	breast:	n/a	n/a
31	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
32	CEBPB	chr4:69325378-69325503	K562	blood:	n/a	n/a
33	CEBPB	chr4:69300055-69300288	A549	lung:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
34	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
35	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr4:69310875-69311174	IMR90	lung:	n/a	chr4:69310996-69311009 chr4:69310996-69311009 chr4:69310996-69311007
37	CEBPB	chr4:69300021-69300356	K562	blood:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
38	CTCF	chr4:69443430-69443586	A549	lung:	n/a	n/a
39	CTCF	chr4:69369324-69369379	GM19238	blood:	n/a	n/a
40	CTCF	chr4:69434848-69435081	A549	lung:	n/a	n/a
41	CTCF	chr4:69364212-69364426	LNCaP	prostate:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
42	CTCF	chr4:69369249-69369482	HepG2	liver:	n/a	n/a
43	CTCF	chr4:69292214-69292221	MCF-7	breast:	n/a	n/a
44	CTCF	chr4:69487398-69487469	Lung_OC	lung:	n/a	n/a
45	CTCF	chr4:69364173-69364466	K562	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
46	CTCF	chr4:69364200-69364350	A549	lung:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
47	CTCF	chr4:69443461-69443509	A549	lung:	n/a	n/a
48	CTCF	chr4:69331900-69332050	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr4:69364100-69364470	ECC-1	luminal epithelium:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
50	CTCF	chr4:69443620-69443770	GM12865	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69435250-69435300	HRCEpiC	kidney:	n/a
2	chr4:69312104-69312154	PFSK-1	brain:	n/a
3	chr4:69313197-69313247	Caco-2	colon:	n/a
4	chr4:69340916-69340966	LNCaP	prostate:	n/a
5	chr4:69435250-69435300	HRCEpiC	kidney:	n/a
6	chr4:69312104-69312154	PFSK-1	brain:	n/a
7	chr4:69313197-69313247	Caco-2	colon:	n/a
8	chr4:69340916-69340966	LNCaP	prostate:	n/a
9	chr4:69435593-69435643	BJ	skin:	n/a
10	chr4:69312104-69312154	CMK	blood:	n/a
11	chr4:69435601-69435651	ovcar-3	ovarian:	n/a
12	chr4:69340916-69340966	HAEpiC	amniotic membrane:	n/a
13	chr4:69313197-69313247	HL-60	blood:	n/a
14	chr4:69381368-69381418	SKMC	muscle:	n/a
15	chr4:69435250-69435300	HAEpiC	amniotic membrane:	n/a
16	chr4:69381368-69381418	NH-A	brain:	n/a
17	chr4:69340916-69340966	AG09319	gingival:	n/a
18	chr4:69312104-69312154	Caco-2	colon:	n/a
19	chr4:69435593-69435643	AoSMC	blood vessel:	n/a
20	chr4:69435593-69435643	SAEC	small airway:	n/a
21	chr4:69434475-69434525	Hela-S3	cervix:	n/a
22	chr4:69340916-69340966	HUVEC	blood vessel:	n/a
23	chr4:69340916-69340966	HNPCEpiC	eye:	n/a
24	chr4:69435601-69435651	HCF	heart:	n/a
25	chr4:69355121-69355171	HCM	heart:	n/a
26	chr4:69340916-69340966	AG09309	skin:	n/a
27	chr4:69434475-69434525	H1-hESC	embryonic stem cell:	embryo
28	chr4:69435250-69435300	HMEC	breast:	n/a
29	chr4:69435593-69435643	NHDF-neo	bronchial:	n/a
30	chr4:69435593-69435643	SKMC	muscle:	n/a
31	chr4:69381368-69381418	HRE	kidney:	n/a
32	chr4:69312104-69312154	NHDF-neo	bronchial:	n/a
33	chr4:69381368-69381418	GM12892	blood:	n/a
34	chr4:69312514-69312564	T-47D	breast:	n/a
35	chr4:69340916-69340966	RPTEC	kidney:	n/a
36	chr4:69381368-69381418	HMEC	breast:	n/a
37	chr4:69381368-69381418	GM12891	blood:	n/a
38	chr4:69435250-69435300	GM19239	blood:	n/a
39	chr4:69435593-69435643	GM12892	blood:	n/a
40	chr4:69313197-69313247	GM12891	blood:	n/a
41	chr4:69381368-69381418	Hela-S3	cervix:	n/a
42	chr4:69381368-69381418	T-47D	breast:	n/a
43	chr4:69435601-69435651	AoSMC	blood vessel:	n/a
44	chr4:69435593-69435643	PrEC	prostate:	n/a
45	chr4:69435593-69435643	SK-N-MC	brain:	n/a
46	chr4:69434475-69434525	HepG2	liver:	n/a
47	chr4:69434475-69434525	T-47D	breast:	n/a
48	chr4:69435593-69435643	HPAEpiC	pulmonary alveolar:	n/a
49	chr4:69312104-69312154	AG04449	skin:	fetal
50	chr4:69434475-69434525	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
2	chr4:69326187..69328959-chr4:69331153..69333884,3	MCF-7	breast:
3	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
4	chr4:69313083..69315969-chr4:69334821..69336429,2	MCF-7	breast:
5	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
6	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
7	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
8	chr4:69319066..69321050-chr4:69325892..69327547,2	MCF-7	breast:
9	chr4:69311298..69314792-chr4:69316366..69319525,5	MCF-7	breast:
10	chr4:69235222..69236888-chr4:69330787..69333108,2	MCF-7	breast:
11	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
12	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
13	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
14	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
15	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
16	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
17	chr4:69308561..69313812-chr4:69314832..69320961,6	K562	blood:
18	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
19	chr4:69317417..69319881-chr4:69327468..69329389,2	MCF-7	breast:
20	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
21	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
2	lnc-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733
3	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736
4	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737
5	lnc-UGT2B17-1	chr4:69382627-69383365	NONHSAT096733
6	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737

Variant related genes	Relation type
TMPRSS11E	TF binding region
ENSG00000249472	TF binding region
ENSG00000251074	TF binding region
ENSG00000251101	TF binding region
UGT2B17	TF binding region
UGT2B29P	TF binding region
TMPRSS11E	CpG island
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B29P	CpG island
ENSG00000249985	chromatin interactions
ENSG00000272626	chromatin interactions
ENSG00000087128	chromatin interactions
ENSG00000083896	chromatin interactions

Extended variants
information (count: 6493 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6493 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537655084	chr4:69287210-69287211	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs146083174	chr4:69287236-69287237	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181685643	chr4:69287250-69287251	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140032468	chr4:69287272-69287273	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149760740	chr4:69287293-69287294	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372228052	chr4:69287321-69287322	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145866821	chr4:69287332-69287333	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186424926	chr4:69287358-69287359	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201646626	chr4:69287365-69287366	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555854157	chr4:69287407-69287408	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149018579	chr4:69287410-69287411	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191077459	chr4:69287453-69287454	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564169710	chr4:69287467-69287468	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs6814549	chr4:69287483-69287484	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577981147	chr4:69287485-69287486	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376536957	chr4:69287488-69287489	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182363299	chr4:69287507-69287508	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186174294	chr4:69287516-69287517	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528899744	chr4:69287567-69287568	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560153794	chr4:69287657-69287658	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528918449	chr4:69287658-69287659	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548980089	chr4:69287686-69287687	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538915718	chr4:69287695-69287696	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562612356	chr4:69287721-69287722	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531347332	chr4:69287722-69287723	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369854174	chr4:69287734-69287735	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551152569	chr4:69287775-69287776	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374011550	chr4:69287791-69287792	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557008942	chr4:69287795-69287796	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374936198	chr4:69287814-69287815	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559630550	chr4:69287832-69287833	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546906827	chr4:69287833-69287834	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369066177	chr4:69287840-69287841	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535847799	chr4:69287917-69287918	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555515382	chr4:69287932-69287933	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142969539	chr4:69287994-69287995	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191044496	chr4:69288014-69288015	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11935742	chr4:69288035-69288036	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs577927037	chr4:69288080-69288081	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540504974	chr4:69288112-69288113	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554111376	chr4:69288113-69288114	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375822948	chr4:69288125-69288126	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370503478	chr4:69288132-69288133	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs137972571	chr4:69288140-69288141	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140714289	chr4:69288143-69288144	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150101010	chr4:69288145-69288146	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138377149	chr4:69288150-69288151	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533373424	chr4:69288172-69288173	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567523529	chr4:69288177-69288178	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149333237	chr4:69288187-69288188	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:455 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69280800-69289600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:69283400-69288000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
3	chr4:69283400-69288000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
4	chr4:69284600-69288000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:69285000-69287800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
6	chr4:69285000-69288000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
7	chr4:69286000-69287400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
8	chr4:69287000-69288000	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr4:69288000-69291600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:69291600-69292400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:69292000-69292200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr4:69292800-69293200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:69293000-69295800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr4:69295600-69296000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr4:69295800-69296600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr4:69295800-69296600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:69296000-69296400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:69296000-69296400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr4:69296000-69296600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:69296400-69300400	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr4:69296400-69300600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr4:69296600-69312000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr4:69298200-69298800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr4:69298800-69300400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr4:69299400-69299600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr4:69299400-69299800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr4:69299800-69300200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr4:69300200-69303400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr4:69300400-69301000	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr4:69300400-69301800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr4:69300400-69302800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr4:69300400-69303400	Enhancers	Primary T cells from cord blood	blood
33	chr4:69300400-69303400	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr4:69300400-69303400	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr4:69300600-69300800	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr4:69300600-69300800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr4:69300600-69301000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:69300600-69302600	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr4:69300600-69302800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr4:69300600-69303400	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr4:69300600-69303400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr4:69300600-69303400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr4:69300800-69301800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr4:69301000-69305800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:69301800-69302000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
46	chr4:69301800-69303200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr4:69301800-69303400	Enhancers	Primary T cells fromperipheralblood	blood
48	chr4:69301800-69307400	Enhancers	Primary B cells from peripheral blood	blood
49	chr4:69302000-69302200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr4:69302200-69302400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood

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